Crystal structures of retaining glycosytransferases

ABSTRACT

The present invention relates to a crystal comprising the ligand binding pocket of a glycosyltransferase enzyme and optionally a donor molecule or analogue thereof and/or an acceptor molecule or analogue thereof. The present invention also relates to the use of such a crystal to identify ligands capable of modulating glycosyltransferase activity, and the use of such ligands in therapeutic applications.

[0001] A portion of the disclosure of this patent document contains material that is subject to copyright protection. The copyright owner has no objection to the facsimile reproduction by anyone of the patent document or patent disclosure, as it appears in the Patent and Trademark Office patent file or records, but otherwise reserves all copyright rights whatsoever.

FIELD OF THE INVENTION

[0002] The present invention relates to crystal structure. In particular a crystal comprising a ligand-binding pocket (LBP) of a glycosyltransferase, optionally having a ligand associated therewith. The invention also relates to a crystal of a retaining glycosyltransferase and parts thereof. In particular, the present invention relates to a crystal comprising a ligand binding pocket of a retaining galactosyltransferase optionally in association with a ligand, for example a donor and/or an acceptor molecule or analogue thereof. The crystals may be useful for modeling and/or synthesizing mimetics of a ligand binding pocket, or ligands that associate with the binding pocket. Such mimetics or ligands may be capable of acting as modulators of glycosyltransferase activity, and they may be useful for treating, inhibiting, or preventing diseases associated with or modulated by glycosyltransferases. The structures may be used to determine retaining glycosyltransferase homologs and information about the secondary and tertiary structures of polypeptides which are as yet structurally uncharacterized.

BACKGROUND

[0003] Oligosaccharides are essential to a wide variety of biological functions many of which are crucial for the development, growth, function and survival of an organism (Varki, 1993 Glycobiology 3, 97-130). Lipooligosaccharide (LOS) is the major glycolipid found on the cell surface of gram-negative mucosal pathogens such as Neisseria, Haemophilus, Moraxella, Bordetella and Campylobacter. The LOS structure is made up of a lipid A moiety, 2-keto-3-deoxyoctulosonic acid (KDO) and various terminal oligosaccharides. Bacterial LOS structures can be antigenically and structurally similar to human glycolipids, and thus may camouflage the bacterial surface from recognition by the human immune system. For example, the terminal structures of N. meningitidis and N. gonorrhoea LOS mimic human lacto-N-neotetraose, sialylacto-N-neotetraose and the P^(k) k blood group glycolipid.

[0004] There have been numerous studies on the genes involved in making the oligosaccharide portion of the LOS structure (Wakarchuk et al, 1996 J. Biol. Chem. 271:19166-19173, Moran et al, 1996 FEMS Immunology and Medical Microbiology 16, 105-115, Kahler & Stephens, 1998 Crit. Rev. Microbiol. 24, 281-334 Biochemical Journal 329, 929-939). An essential aspect of this biosynthesis involves the linking of saccharides with the aid of glycosyltransferases (for classification of the distinct families see Campbell et al., 1997 Biochemical Journal 326, 929-939). These enzymes transfer a sugar, mainly from a nucleotide diphospho-sugar, but also from sugar phosphates, to specific acceptor molecules. α-1, 4-Galactosyltransferase from N. meningitidis (Family 8 in the scheme of Campell et al., 1997 as above), adds an α-galactose from UDPgal (the donor) to a terminal lactose (the acceptor) of the LOS structure creating the P^(k) blood group glycolipid mimic (FIG. 1a). Interest in understanding this and other bacterial transferases stems, at least in part, from the notion that inhibitors that block the essential formation of LOS biosynthesis in pathogenic bacteria may prove to be useful new antibiotics (Takayama et al, 1999 Bioorganic and Medicinal Chemistry 7, 401-409).

[0005] Based on the relative anomeric stereochemistries of the substrate and product in the reaction catalyzed, glycosyltransferases can be classified mechanistically as either inverting or retaining, (as is also done with the well-studied glycosidase family; Sinnott, 1990, Chem. Rev., 90, 1171-1202; Davies et al., 1997 in Comprehensive Biological Catalysis (Sinnott, M. L., ed) Vol. 1, pp. 119-208, Academic Press, London; Zechel & Withers, 2000 Acc. Chem. Res. 33, 11-18). While this has led to the tacit assumption that similar mechanisms are employed by glycosidases and glycosyltransferases in carrying out their functions, very little has been experimentally verified about the mechanism of the latter.

[0006] By simple analogy with the glycosidase counterpart, inverting glycosyltransferases are believed to follow a direct displacement mechanism with a general base to assist in deprotonating the reactive hydroxyl of the acceptor molecule and possibly a general acid to aid in cleavage of the exocyclic C₁—O bond, though a bound metal ion may fulfil this role (FIG. 1b). In the case of retaining transferases, catalysis is believed to proceed via a double displacement mechanism involving the formation and subsequent breakdown of a covalent glycosyl-enzyme intermediate (FIG. 1c). In such a scheme, a nucleophile is required for attack on the anomeric centre of the donor sugar to form the glycosyl-enzyme species. Once again, either an acid catalyst or a metal ion will be required to provide general acid assistance to the cleavage of the exocyclic C₁—O bond (in the first step) and a general base will be needed to deprotonate the reactive hydroxyl of the acceptor molecule (in the second step).

[0007] To date the x-ray crystal structures of only four glycosyltransferases have been determined and all catalyze inverting reactions; β-glucosyltransferase from phage T4, (Vrielink et al.,1994 EMBO J. 13, 3413-3422), SpsA from Bacillus subtilis (Charnock and Davies, 1999 Biochemistry. 38, 6380-6385.), bovine β-1,4-galactosyltransferase (Gastinel et al., 1999) and MurG from E. coli (Ha et al, 2000). With the exception of MurG, these structures have been determined in complex with UDP or the donor UDP-sugar. However, electron density for the sugar moiety has not been observed in any of these experiments.

[0008] Despite the fact that the biosynthesis of polysaccharides is of fundamental biological importance, and that a large number of glycosyltransferases have already been described, to date no crystal structures have been provided for retaining glycosyltransferase enzymes, and no crystal structures of any glycosyltransferase enzymes have been provided which give any structural data for the donor and/or acceptor molecule.

[0009] Such crystal structures would be invaluable in understanding the catalytic mechanism of the enzymes and in the rational design of inhibitors.

SUMMARY OF THE INVENTION

[0010] The present invention is based on the finding that it is possible to crystallize a retaining glycosyltransferase, both alone and in combination with a selection of different ligands. More particularly, Applicants have crystallized a retaining glycosyltransferase in complex with a metal cofactor, a donor molecule, and in the presence or absence of an acceptor molecule, and have solved the three-dimensional structure of the enzyme. Solving the crystal structure has enabled the determination of key structural features of retaining glycosyltransferases, particularly the shape of ligand binding pockets (also referred to herein as “LBP”), or parts thereof, that associate with a metal cofactor, donor molecule, and/or acceptor molecule. The crystal structure has also enabled the determination of key structural features in donor molecules and acceptor molecules.

[0011] Binding pockets are of significant utility in drug discovery. The association of natural ligands and substrates with the binding pockets of their corresponding glycosyltransferases is the basis of many biological mechanisms. In addition, many drugs exert their effects through association with the binding pockets of glycosyltransferases. The associations may occur with all or any parts of a binding pocket An understanding of these associations will lead to the design and optimization of drugs having more favorable associations with their target glycosyltransferase and thus provide improved biological effects. Therefore, information about the shape and structure of glycosyltransferases and their ligand-binding pockets is invaluable in designing potential modulators of glycosyltransferases for use in treating diseases and conditions associated with or modulated by the glycosyltransferases.

[0012] Therefore, broadly stated the present invention relates to the secondary, tertiary, and/or quanternary structures of glycosyltransferases, and parts thereof. The glycosyltransferase structure may be the structure the enzyme forms when it is associated with one or more ligands (e.g. an acceptor molecule, a donor molecule, or components thereof). The invention also contemplates a glycosyltransferase structure comprising a the secondary, tertiary, and/or quanternary structure of a glycosyltransferase in association with a ligand. The defined boundaries and properties of the structures and any of the ligands bound to it are pertinent to methods for determining the secondary, tertiary, and/or quanternary structures of polypeptides with unknown structure, and to methods that identify modulators of glycosyltansferases. These modulators are potentially useful as therapeutics for diseases associated with or modulated by glycosytransferases.

[0013] In an embodiment, the invention provides a crystal of a polypeptide corresponding to a retaining glycosyltransferase, or a part thereof (e.g. ligand binding pocket). The invention preferably contemplates the crystal a retaining glycosyltransferase forms when it is complexed with a ligand, including a donor molecule or analogue thereof, an acceptor molecule or analogue thereof, a metal cofactor, and/or heavy metal atom. The crystal form may also comprise one or more ligands (e.g. donor molecule or acceptor molecule).

[0014] A glycosyltransferase structure of the invention may be characterized by the following:

[0015] (a) a ligand binding pocket comprising a core β-sheet containing 7 strands (β33, β2, β1, β4, β6, β8 in FIG. 3) all of which are parallel with the exception of β7; the core β-sheet being further characterized by a nucleotide binding motif composed of four parallel strands sandwiched between helices A and B on one side and helices C and D on the other as illustrated in FIG. 3;

[0016] (b) an antiparallel β-ribbon formed by two strands (β5 and β9) lying almost perpendicular to the core β-sheet, and a substrate binding cleft that lies along the base of the core β-sheet; or

[0017] (c) a C-terminal domain mediating membrane attachment comprising helix M and Helix N in FIG. 3 forming a small pedestal that packs perpendicular to helices A and B of the nucleotide binding motif and to the β-ribbon as shown in FIG. 3.

[0018] The present invention also contemplates molecules or molecular complexes that comprise all or parts of either one or more ligand binding pockets, or homologues of these ligand binding pockets that have similar three-dimensional shapes.

[0019] According to an aspect of the invention there is provided a crystal comprising a ligand binding pocket of a retaining glycosyltransferase.

[0020] A ligand binding pocket may include one or more of the binding domains for a disphosphate group or pyrophosphate of a donor molecule, a nucleotide of a donor molecule, a nitrogeneous heterocyclic base (preferably a pyrimidine base, more preferably uracil) of a donor molecule, a sugar of the nucleotide of a donor molecule, a selected sugar of a donor molecule that is transferred to an acceptor molecule, and/or an acceptor molecule.

[0021] The present invention also provides a crystal comprising a ligand binding pocket of a retaining glycosyltransferase and a donor molecule or analogue thereof from which it is possible to derive structural data for the donor molecule or analogue thereof.

[0022] The present invention also provides a crystal comprising a ligand binding pocket of a retaining glycosyltransferase and an acceptor molecule or analogue thereof from which it is possible to derive structural data for the acceptor molecule or analogue thereof.

[0023] The present invention also provides a crystal comprising the ligand binding pocket of a retaining glycosyltransferase and a metal cofactor.

[0024] In an embodiment a crystal of the invention comprises a ligand binding pocket in association with or complexed with a donor molecule or analogue thereof and/or an acceptor molecule or analogue thereof. In another embodiment the ligand binding pocket is associated with or complexed with a donor molecule, a metal cofactor, and an acceptor molecule. These crystals make it possible to derive structural data for a donor molecule or an acceptor molecule, or analogues thereof.

[0025] The shape and structure of a ligand binding pocket may be defined by selected atomic contacts in the pocket In an embodiment the ligand binding pocket is defined by one or more atomic interactions or enzyme atomic contacts as set forth in Table 3. Each of the atomic interactions is defined in Table 3 by an atomic contact (more preferably, a specific atom where indicated) on the donor molecule or analogue thereof or acceptor molecule or analogue thereof, and an atomic contact (more preferably a specific atom where indicated) on the glycosyltransferase.

[0026] In an embodiment, the ligand binding pocket is an active site binding pocket of a glycosyltransferase. The active site binding pocket refers to the region of a glycosyltransferase where the transfer of a sugar from the donor molecule to the acceptor occurs.

[0027] The invention also provides a method for crystallizing a retaining glycosyltransferase, or a part thereof (e.g. ligand binding pocket), or a complex of a retaining glycosyltransferase or a part thereof and a metal cofactor, donor molecule, and/ or acceptor molecule.

[0028] The crystal structures of the invention enable a model to be produced for a glycosyltransferase and a part thereof, (e.g. a ligand binding pocket), or complexes of the enzyme or parts thereof The models may provide structural information about the donor and/or acceptor molecule and their interactions with the LBP. Models may also be produced for donor and acceptor molecules.

[0029] Therefore the invention also provides a model of a ligand binding pocket designed in accordance with a method of the invention. The invention contemplates a model, crystal, or secondary, tertiary and/or quanternary structure of a glycosyltransferase or ligand binding pocket in association with a ligand or substrate.

[0030] The structures and models of the invention provide information about the atomic contacts involved in the interaction between the enzyme and a known ligand which can be used to screen for unknown ligands. Therefore the present invention provides a method of screening for a ligand capable of binding a glycosyltransferase ligand binding domain, comprising the use of a secondary, tertiary or quanternary structure or a model of the invention. For example, the method may comprise the step of contacting a ligand binding domain with a test compound, and determining if the test compound binds to the ligand.

[0031] A crystal and/or model of the invention may be used in a method of determining the secondary, tertiary, and/or quanternary structures of a polypeptide with incompletely characterised structure. Thus, a method is provided for determining at least a portion of the secondary, tertiary, and/or quanternary structure of molecules or molecular complexes which contain at least some structurally similar features to a retaining glycosyltransferase. This is achieved by using at least some of the structural coordinates set out in Table 4, 5 or 6.

[0032] A structure, crystal and/or model of the invention may be used to design, evaluate, and identity ligands of a glycosyltransferases or homologues thereof. A ligand may be based on the shape and structure of a glycosyltransferase, or a ligand binding pocket or atomic interactions, or atomic contacts thereof. Preferably, a ligand is derived from a ligand binding pocket for a donor molecule or analogue or parts thereof, and/or an acceptor molecule or analogue or parts thereof. The invention also provides modulators that are derived from a DXD motif or the C-terminal binding pocket mediating membrane attachment.

[0033] The present invention also contemplates a ligand identified by a method of the invention. A ligand may be a competitive or non-competitive inhibitor of a glycosyltransferase. Preferably, the ligand is a modulator that is capable of modulating the activity of a glycosyltransferase enzyme. Thus, the methods of the invention permit the identification early in the drug development cycle of compounds that have advantageous properties.

[0034] In an embodiment, the present invention contemplates a method of identifying a modulator of a glycosyltransferase, or a ligand binding pocket, or a part thereof, comprising the step of applying the structural coordinates of a glycosyltransferase, ligand binding pocket, or atomic interactions, or atomic contacts thereof, to computationally evaluate a test ligand for its ability to associate with the glycosyltransferase, or ligand binding pocket, or part thereof. Use of the structural coordinates of a glycosyltransferase structure or ligand binding pocket, or atomic interactions, or atomic contacts thereof to identify a modulator is also provided.

[0035] In an embodiment, the present invention contemplates a method of identifying a modulator of a glycosyltransferase or a ligand binding pocket or binding site thereof, comprising the step of using the structural coordinates of a glycosyltransferase or a ligand binding pocket or binding site thereof, or a model of the invention to computationally evaluate a test compound for its ability to associate with the glycosyltransferase or ligand binding pocket or binding site thereof. Use of the structural coordinates of a glycosyltransferase structure, ligand binding pocket, or binding site thereof, of the invention to identify a ligand or modulator is also provided.

[0036] In another embodiment of the invention, a method is provided for identifying a potential modulator of a glycosyltransferase by determining binding interactions between a test compound and atomic contacts of a ligand binding pocket of a glycosyltransferase defined in accordance with the invention comprising:

[0037] (a) generating the atomic contacts on a computer screen;

[0038] (b) generating test compounds with their spatial structure on the computer screen; and

[0039] (c) determining whether the compounds associate or interact with the atomic contacts defining the glycosyltransferase;

[0040] (d) identifying test compounds that are potential modulators by their ability to enter into, a selected number of atomic contacts.

[0041] Another aspect of the invention provides methods for identifying a potential modulator of a glycosyltransferase function by docking a computer representation of a test compound with a computer representation of a structure of a glycosyltransferase or a ligand binding pocket thereof that is defined as described herein. In an embodiment the method comprises the following steps:

[0042] (a) docking a computer representation of a compound from a computer data base with a computer representation of atomic interactions or atomic contacts of a ligand binding pocket of a glycosyltransferase to obtain a complex;

[0043] (b) determining a conformation of the complex with a favourable geometric fit and favourable complementary interactions; and

[0044] (c) identifying test compounds that best fit the atomic interactions or contacts as potential modulators of the glycosyltransferase.

[0045] In another embodiment the method comprises the following steps:

[0046] (a) modifying a computer representation of a test compound complexed with a ligand binding pocket of a glycosyltransferase by deleting or adding a chemical group or groups;

[0047] (b) determining a conformation of the complex with a favourable geometric fit and favourable complementary interactions; and

[0048] (c) identifying a test compound that best fits the ligand binding pocket as a potential modulator of a glycosyltransferase.

[0049] In still another embodiment the method comprises the following steps:

[0050] (a) generating a computer representation of a test compound complexed with atomic contacts or atomic interactions of a binding pocket of a glycosyltransferase; and

[0051] (b) searching for molecules in a data base that are similar to the test compound using a searching computer program, or replacing portions of the test compound with similar chemical structures from a data base using a compound building computer program.

[0052] The ligands or compounds identified according to the methods of the invention preferably have structures such that they are able to enter into an association with a ligand binding pocket Selected ligands or compounds may be characterized by their suitability for binding to particular ligand binding pockets. A ligand binding pocket or binding site may be regarded as a type of negative template with which the compounds correlate as positives in the manner described herein and thus the compounds are unambiguously defined. Therefore, it is possible to describe the structure of a compound suitable as a modulator of a glycosyltransferase by accurately defining the atomic interactions to which the compound binds to a ligand binding pocket and deriving the structure of the compound from the spacial structure of the target.

[0053] The invention contemplates a method for the design of ligands, in particular modulators, for glycosyltransferase based on the secondary, tertiary or quanternary structure of a donor molecule or acceptor molecule (or part thereof) defined in relation to its spatial association with the three dimensional structure of the glycosyltransferase or a ligand binding pocket thereof. Generally, a method is provided for designing potential inhibitors of a glycosyltransferase comprising the step of using the structural coordinates of a donor molecule or acceptor molecule or part thereof, defined in relation to its spatial association with the secondary, tertiary or quanternary structure or model of a glycosyltransferase or a ligand binding pocket thereof, to generate a compound for associating with the ligand binding pocket of the glycosyltransferase. The following steps are employed in a particular method of the invention: (a) generating a computer representation of a donor molecule or acceptor molecule, or part thereof, defined in relation to its spatial association with the three dimensional structure of a glycosyltransferase or a ligand binding pocket thereof, or defined by the structural coordinates shown in Table 4, 5, or 6; (b) searching for molecules in a data base that are similar to the defined donor molecule or acceptor molecule, or part thereof using a searching computer program, or replacing portions of the compound with similar chemical structures from a database using a compound building computer program.

[0054] Therefore, the invention further contemplates classes of ligands, in particular modulators, of a glycosyltransferase based on the secondary, tertiary or quanternary structure of a donor molecule or acceptor molecule, or part thereof, defined in relation to the donor or acceptor molecule's spatial association with a three dimensional structure of a glycosyltransferase.

[0055] It will be appreciated that a modulator of a glycosyltransferase may be identified by generating an actual secondary or three-dimensional model of a ligand binding pocket, synthesizing a compound, and examining the components to find whether the required interaction occurs.

[0056] A potential ligand or modulator of a glycosyltransferase identified by a method of the present invention may be confirmed as a modulator by synthesizing the compound, and testing its effect on the glycosyltransferase in an assay for that glycosyltransferase's enzymatic activity. Such assays are known in the art. (See for example, Sadler, J. E. et al. Methods Enzymol., 83, 458-514; Schachter, H., et al Methods Enzymol., 179, 351-397; Datti, A., et al Anal.Biochem., 206, 262-266; Palcic, M. M. (1994) Methods Enzymol., 230, 300-316; Fitzgerald, D. K., et al, Anal.Biochem., 36, 43-61; Gosselin, S., et al Anal.Biochem., 220, 92-97; Crawley, S. C., et al Anal.Biochem 185, 112-117; Yan, L., et al, Anal.Biochem., 223, 111-118; Yeh, J. C. and Cummings, R. D. (1996) Anal.Biochem., 236, 126-133; DeBose-Boyd, R. A., et al Arch.Biochem.Biophys., 335, 109-117; Rabina, J., et al, Anal.Biochem., 246, 71-78; Shedletzky, E., et al Anal.Biochem., 249, 88-93; Oubihi, M., et al Anal.Biochem., 257, 169-175; Kanie, Y., et al Anal.Biochem., 263, 240-245.)

[0057] A ligand or modulator of the invention may be converted using customary methods into pharmaceutical compositions. A ligand or modulator may be formulated into a pharmaceutical composition containing a ligand or modulator either alone or together with other active substances.

[0058] Ligands that are modulators that are capable of modulating the activity of glycosyltransferases have therapeutic and prophylactic potential. Therefore, the methods of the invention for identifying ligands or modulators may comprise one or more of the following additional steps:

[0059] (a) testing whether the ligand is a modulator of the activity of a glycosyltransferase, preferably testing the activity of the ligand in cellular assays and animal model assays;

[0060] (b) modifying the ligand;

[0061] (c) optionally rerunning steps (a) or (b); and

[0062] (d) preparing a pharmaceutical composition comprising the ligand.

[0063] Steps (a), (b) (c) and (d) may be carried out in any order, at different points in time, and they need not be sequential.

[0064] Still another aspect of the invention provides a method of conducting a drug discovery business comprising:

[0065] (a) providing one or more systems or methods for identifying modulators based on a model or structure of the present invention, preferably a method using a computer as described herein;

[0066] (b) conducting therapeutic profiling of modulators identified in step (a), or further analogs thereof, for efficacy and toxicity in animals; and

[0067] (c) formulating a pharmaceutical composition including one or more agents identified in step (b) as having an acceptable therapeutic profile.

[0068] In certain embodiments, the subject method may also include a step of establishing a distribution system for distributing the pharmaceutical composition for sale, and may optionally include establishing a sales group for marketing the pharmaceutical composition.

[0069] In yet another aspect of the invention, a method of conducting a target discovery business is provided comprising:

[0070] (a) providing one or more system or method for identifying modulators based on a model or structure of the present invention, preferably a method using a computer as described herein;

[0071] (b) optionally conducting therapeutic profiling of modulators identified in (a) for efficacy and toxicity in animals; and

[0072] (c) licensing to a third party the rights for further drug development and/or sales for agents identified in step (a), or analogs thereof.

[0073] There is also provided a pharmaceutical composition comprising a ligand or modulator, and a method of treating and/or preventing disease associated with a glycosyltransferase comprising the step of administering a ligand or modulator or pharmaceutical composition comprising a modulator to a patient.

[0074] In an aspect, the invention contemplates a method of treating a disease associated with a glycosyltransferase with inappropriate activity in a cellular organism, comprising:

[0075] (a) administering a ligand or modulator identified using the methods of the invention in an acceptable pharmaceutical preparation; and

[0076] (b) activating or inhibiting a glycosyltransferase to treat the disease.

[0077] The invention provides for the use of a ligand or modulator identified by the methods of the invention in the preparation of a medicament to treat or prevent a disease associated with or modulated by a glycosyltransferase in a cellular organism. Use of ligands or modulators of the invention to manufacture a medicament is also provided.

[0078] Another aspect of the invention provides machine readable media encoded with data representing a crystal or model of the invention or the coordinates of a structure of a glycosyltransferase or ligand binding pocket or binding site thereof as defined herein, or the three dimensional structure of a donor molecule or acceptor molecule or part thereof defined in relation to its spatial association with a three dimensional structure of a glycosyltransferase as defined herein. The invention also provides computerized representations of a crystal or model of the invention or the secondary, tertiary or quanternary structures of the invention, including any electronic, magnetic, or electromagnetic storage forms of the data needed to define the structures such that the data will be computer readable for purposes of display and/or manipulation. The invention further provides a computer programmed with a homology model of a ligand binding pocket of a glycosyltransferase. The invention still further contemplates the use of a homology model of the invention as input to a computer programmed for drug design and/or database searching and/or molecular graphic imaging in order to identify new ligands or modulators for glycosyltransferases.

[0079] These and other aspects of the present invention will become evident upon reference to the following detailed description and Tables, and attached drawings.

DESCRIPTION OF THE DRAWINGS

[0080] The present invention will now be described only by way of example, in which reference will be made to the following Figures:

[0081]FIG. 1. Glycosyl transfer reactions. a) The LgtC catalyzed transfer of galactose from UDP-Gal to the LPS core oligosaccharide of Neisseria. The proposed mechanisms of b) an inverting and c) a retaining α-galactosyltransferase.

[0082]FIG. 2. An amino acid sequence alignment of Neisseria meningitidis LgtC and related enzymes from glycosyl transferase family 8. Secondary structure elements of LgtC are indicated above the sequence. Invariant residues are shown on blue background and conserved on orange. Sequences from the following organisms were used, their accession numbers in parenthesis. Neisseria meningitidis (P96945), Neisseria gonorrheae (Q50948), Pasturella multocida (AF237927), Haemophilus influenzae (P43947), Escherichia coli (Q92155), Salmonella tryphimurium (P19816), Helicobacter pylori (024967). Residues interacting with the UDP portion of the donor or with the galactose part are marked with filled circles and triangles respectively. Residues coordinating the metal are marked with stars and those that interact with 4-deoxylactose with diamonds.

[0083]FIG. 3. The overall architecture of LgtC. 3A. A C-α trace of the Lgtc monomer shown in stereo. 3B. The LgtC structure with bound substrate analogues. The substrates are depicted in CPK representation where the acceptor is coloured dark gray, the donor light gray and the manganese pink. Strands and helices are labelled. 3C. View of the LgtC structure showing the substrate binding N-terminal domain and the membrane attaching C-terminal domain. 3D. Topology diagram of LgtC. Helices are coloured blue and strands green.

[0084]FIG. 4. Stereo view of the active site. 4A. The ball-and stick models of the donor sugar UDP-Gal is colored as red sticks and the acceptor sugar lactose as green sticks in a refined 2fo-fc map contoured at 1.2 sigma. Amino acids interacting with the substrates are labeled. The loops that fold over the active site, residues 75-80 and 246-251, are colored in green. 4B. Molecular surface representation of the active site. UDP-Gal and 4-deoxylactose are shown in ball-and-stick form. UDP-Gal is almost completely buried in the enzyme while 4-deoxylactose is bound in an open pocket, more accessible to solvent 4C. The hydrogen bonding network of Q189 and the distance and angle to the anomeric carbon C1′.Distances are in Å.

[0085]FIG. 5. Schematic representation of the interactions between the enzyme and the substrate analogues. Hydrogen bonds (<3.1 Å for all bonds except Cys; <3.5 Å) are indicated with dashed lines. Vdw contacts are shown as nested half circles. Water molecules have not been included.

[0086]FIG. 6. Possible mechanisms in the LgtC catalyzed reaction. a) 6′-OH of the acceptor substrate and the b) side chain amide oxygen of Gln189 as potential nucleophiles. c) The mechanism of a hexosaminidase in which the amide oxygen of the substrate has been shown to function as the catalytic nucleophile.

DESCRIPTION OF THE TABLES

[0087] The present invention will now be described only by way of example, in which reference will be made to the following Tables:

[0088] Table 1 shows a specific comparison of the specific activity and kinetic parameters of the mutants to the wild-type protein

[0089] Table 2 shows data collection, refinement statistics, and model steriochemistry.

[0090] Table 3 shows atomic interactions of a retaining glycosyltransferase and a donor molecule, and an acceptor molecule.

[0091] Table 4 shows the structural coordinates of a retaining galactosyltransferase LgtC from Neisseria meningitidis in complex with manganese and UDP 2-deoxy-2-fluoro-galactose.

[0092] Table 5 shows the structural coordinates of a retaining galactosyltransferase LgtC from Neisseria meningitidis in complex with manganese, UDP 2-deoxy-2-fluoro-galactose and 4-deoxylactose.

[0093] Table 6 shows the structural coordinates of a retaining galactosyltransferase LgtC from Neisseria meningitidis in complex with manganese and UDP 2-deoxy-2-fluoro-galactose and lactose.

[0094] In Tables 4 through 6 inclusive, from the left, the second column identifies the atom number; the third identifies the atom type; the fourth identifies the amino acid type; the fifth identifies the residue number; the sixth identifies the x coordinates; the seventh identifies the y coordinates; and the eighth identifies the z coordinates.

DETAILED DESCRIPTION OF THE INVENTION

[0095] Unless otherwise indicated, all terms used herein have the same meaning as they would to one skilled in the art of the present invention. Practitioners are particularly directed to Current Protocols in Molecular Biology (Ansubel) for definitions and terms of the art.

[0096] Glycosyltransferase

[0097] The invention generally relates to glycosyltransferases and parts thereof. A glycosyltransferase enzyme is capable of transferring a particular sugar residue from a donor molecule to an acceptor molecule, thus forming a glycosidic linkage. Based on the type of donor sugar transferred, these enzymes are grouped into families, e.g. N-acetylglucosaminyltansferases, N-acetylgalactosaminyltransferases, mannosyltransferases, fucosyltransferases, galactosyltransferases, and sialyltransferases.

[0098] A retaining glycosyltransferases is one which transfers a sugar residue with the retention of anomeric configuration. An inverting glycosyltransferase, on the other hand, is one which transfers a sugar residue with the inversion of anomeric configuration. Campbell et al (1997) (as above) describes a classification of glycosyltransferases based on amino acid sequence similarities. Twenty-six families have been identified altogether, thirteen of which are designated as being inverting enzymes (Families 1, 2, 7, 9, 10, 11, 12, 13, 14, 16, 17, 18 and 23) and eight of which are designated as being retaining enzymes (Families 3, 4, 5, 6, 8, 15, 20 and 21).

[0099] In accordance with certain aspects of the invention, the enzyme is a retaining glycosyltransferase of Family 3, 4, 5, 6, 8, 15, 20 and 21 in the scheme of Campbell et al. In an aspect of the invention the enzyme is capable of catalyzing a step in the biosynthesis of a lipooligosaccharide or lipopolysaccharide. Preferably the glycosyltransferase is a member of Family 8 and has the activities of a lipopolysaccharide galactosyltransferase (EC 2.4.1.44), lipopolysaccharide glucosyltransferase 1 (EC 2.4.1.58), glycogenin glucosyltransferase (EC 2.4.1.186), inositol 1-α galactosyltransferase (EC 2.4.1.123). In a more preferred embodiment, the enzyme is a lipopolysaccharide galactosyltransferase [e.g. SwissProt P27128 (E. coli rfaI) and P19816 (S. typhimurium rfaI)] and in a most preferred embodiment the enzyme is a lipopolysaccharide galactosyltransferase of Neisseria (e.g. meningitidis, gonorrhoeae). A highly preferably enzyme is an α 1,4-galactosyltransferase from Neisseria menigitidis (GenBank Accession No. U65788).

[0100] Glycosyltransferases are derivable from a variety of sources, including viruses, bacteria, fungi, plants and animals. In a preferred embodiment the glycosyltransferase is derivable from a bacterium, in particular a gram-negative bacterium, such as one which is capable of acting as a pathogen. In an aspect of the invention the enzyme is derivable form a gram negative mucosal pathogen. For example, the glycosyltanferase may be found in one (or more) of the following organisms: Neisseria, Escherichia, Salmonella, Haemophilus, Moraxella, Bordatella, and Campylobacter. In a preferred embodiment the enzyme is found in a bacteria of the genus Neisseria, for example N. meningitidis or N. gonorrhea. In a highly preferred embodiment, the enzyme is found in N. meningitidis.

[0101] Preferably the glycosyltransferase is derivable from an organism possessing a lipooligosaccharide (LOS). The lipooligosaccharide may mimic human glycolipids in order to avoid detection by the immune system. For example, the LOS may mimic human lacto-N-neotetraose, sialylacto-N-neotetraose and/or the P^(k) blood group glycolipid. In a highly preferred embodiment, the enzyme is capable of adding an α-galactose to a terminal lactose of the LOS structure, creating a P^(k) blood group glycolipid mimic.

[0102] A glycosyltransferase or part thereof in the present invention may be a wild type enzyme, or part thereof, or a mutant, variant or homologue of such an enzyme.

[0103] The term “wild type” refers to a polypeptide having a primary amino acid sequence which is identical with the native enzyme (for example, the bacterial enzyme).

[0104] The term “mutant” refers to a polypeptide having a primary amino acid sequence which differs from the wild type sequence by one or more amino acid additions, substitutions or deletions. Preferably, the mutant has at least 90% sequence identity with the wild type sequence. Preferably, the mutant has 20 mutations or less over the whole wild-type sequence. More preferably the mutant has 10 mutations or less, most preferably 5 mutations or less over the whole wild-type sequence. A mutant may or may not be functional.

[0105] The term “variant” refers to a naturally occurring polypeptide which differs from a wild-type sequence. A variant may be found within the same species (i.e. if there is more than one isoform of the enzyme) or may be found within a different species. Preferably the variant has at least 90% sequence identity with the wild type sequence. Preferably, the variant has 20 mutations or less over the whole wildtype sequence. More preferably, the variant has 10 mutations or less, most preferably 5 mutations or less over the whole wild-type sequence.

[0106] The term “part” indicates that the polypeptide comprises a fraction of the wild-type amino acid sequence. It may comprise one or more large contiguous sections of sequence or a plurality of small sections. The “part” may comprise a ligand binding pocket as described herein. The polypeptide may also comprise other elements of sequence, for example, it may be a fusion protein with another protein (such as one which aids isolation or crystallisation of the polypeptide). Preferably the polypeptide comprises at least 50%, more preferably at least 65%, most preferably at least 80% of the wild-type sequence.

[0107] The term “homologue” means a polypeptide having a degree of homology with the wild-type amino acid sequence. The term “homology” can be equated with “identity”.

[0108] In the present context, a homologous sequence is taken to include an amino acid sequence which may be at least 75, 85 or 90% identical, preferably at least 95 or 98% identical to the wild-type sequence. Typically, the homologues will comprise the same sites (for example LBP) as the subject amino acid sequence. Although homology can also be considered in terms of similarity (i.e. amino acid residues having similar chemical properties/functions), in the context of the present invention it is preferred to express homology in terms of sequence identity.

[0109] Homology comparisons can be conducted by eye, or more usually, with the aid of readily available sequence comparison programs. These commercially available computer programs can calculate % homology between two or more sequences (e.g. Wilbur, W. J. and Lipman, D. J. Proc. Natl. Acad. Sci. USA (1983), 80:726-730).

[0110] Percentage homology may be calculated over contiguous sequences, i.e. one sequence is aligned with the other sequence and each amino acid in one sequence is directly compared with the corresponding amino acid in the other sequence, one residue at a time. This is called an “ungapped” alignment. Typically, such ungapped alignments are performed only over a relatively short number of residues.

[0111] Although this is a very simple and consistent method, it fails to take into consideration that, for example, in an otherwise identical pair of sequences, one insertion or deletion will cause the following amino acid residues to be put out of alignment, thus potentially resulting in a large reduction in % homology when a global alignment is performed. Consequently, most sequence comparison methods are designed to produce optimal alignments that take into consideration possible insertions and deletions without penalising unduly the overall homology score. This is achieved by inserting “gaps” in the sequence alignment to try to maximise local homology.

[0112] However, these more complex methods assign “gap penalties” to each gap that occurs in the alignment so that, for the same number of identical amino acids, a sequence alignment with as few gaps as possible—reflecting higher relatedness between the two compared sequences—will achieve a higher score than one with many gaps. “Affine gap costs” are typically used that charge a relatively high cost for the existence of a gap and a smaller penalty for each subsequent residue in the gap. This is the most commonly used gap scoring system. High gap penalties will of course produce optimised alignments with fewer gaps. Most alignment programs allow the gap penalties to be modified. However, it is preferred to use the default values when using such software for sequence comparisons. For example when using the GCG Wisconsin Bestfit package the default gap penalty for amino acid sequences is −12 for a gap and −4 for each extension.

[0113] Calculation of maximum % homology therefore firstly requires the production of an optimal alignment, taking into consideration gap penalties. A suitable computer program for carrying out such an alignment is the GCG Wisconsin Bestfit package (University of Wisconsin, U.S.A.; Devereux et al., 1984, Nucleic Acids Research 12:387). Examples of other software than can perform sequence comparisons include, but are not limited to, the BLAST package (see Ausubel et al., 1999 ibid—Chapter 18), FASTA (Atschul et al., 1990, J. Mol. Biol., 403-410) and the GENEWORKS suite of comparison tools. Both BLAST and FASTA are available for offline and online searching (see Ausubel et al., 1999 ibid, pages 7-58 to 7-60). However, for some applications, it is preferred to use the GCG Bestfit program. A new tool, called BLAST 2 Sequences is also available for comparing protein and nucleotide sequence (see FEMS Microbiol Lett 1999 174(2): 247-50; FEMS Microbiol Lett 1999 177(1): 187-8 and tatiana@ncbi.nln.nih.gov).

[0114] Although the final % homology can be measured in terms of identity, the alignment process itself is typically not based on an all-or-nothing pair comparison. Instead, a scaled similarity score matrix is generally used that assigns scores to each pairwise comparison based on chemical similarity or evolutionary distance. An example of such a matrix commonly used is the BLOSUM62 matrix—the default matrix for the BLAST suite of programs. GCG Wisconsin programs generally use either the public default values or a custom symbol comparison table if supplied (see user manual for further details). For some applications, it is preferred to use the public default values for the GCG package, or in the case of other software, the default matrix, such as BLOSUM62.

[0115] Once the software has produced an optimal alignment, it is possible to calculate % homology, preferably % sequence identity. The software typically does this as part of the sequence comparison and generates a numerical result.

[0116] The sequences may have deletions, insertions or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent enzyme. Deliberate amino acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues as long as the secondary binding activity of the substance is retained. For example, negatively charged amino acids include aspartic acid and glutamic acid; positively charged amino acids include lysine and arginine; and amino acids with uncharged polar head groups having similar hydrophilicity values include leucine, isoleucine, valine, glycine, alanine, asparagine, glutamine, serine, threonine, phenylalanine, and tyrosine.

[0117] Conservative substitutions may be made, for example according to the Table below. Amino acids in the same block in the second column and preferably in the same line in the third column may be substituted for each other: ALIPHATIC Non-polar G A P I L V Polar - uncharged C S T M N Q Polar - charged D E K R AROMATIC H F W Y

[0118] The polypeptide may also have a homologous substitution (substitution and replacement are both used herein to mean the interchange of an existing amino acid residue, with an alternative residue) i.e. like-for-like substitution such as basic for basic, acidic for acidic, polar for polar etc. Non-homologous substitution may also occur i.e. from one class of residue to another or alternatively involving the inclusion of unnatural amino acids such as ornithine (hereinafter referred to as Z), diaminobutyric acid ornithine (hereinafter referred to as B), norleucine ornithine (hereinafter referred to as O), pyriylalanine, thienylalanine, naphthylalanine and phenylglycine.

[0119] Replacements may also be made by unnatural amino acids include; alpha* and alpha-disubstituted* amino acids, N-alkyl amino acids*, lactic acid*, halide derivatives of natural amino acids such as trifluorotyrosine*, p-Cl-phenylalanine*, p-Br-phenylalanine*, p-I-phenylalanine*, L-allyl-glycine*, β-alanine*, L-a-amino butyric acid*, L-γ-amino butyric acid*, L-α-amino isobutyric acid*, L-ε-amino caproic acid#, 7-amino heptanoic acid*, L-methionine sulfone#*, L-norleucine*, L-norvaline*, p-nitro-L-phenylalanine*, L-hydroxyproline#, L-thioproline*, methyl derivatives of phenylalanine (Phe) such as 4-methyl-Phe*, pentamethyl-Phe*, L-Phe (4-amino), L-Tyr (methyl)*, L-Phe (4-isopropyl)*, L-Tic (1,2,3,4-tetrahydroisoquinoline-3-carboxyl acid)*, L-diaminopropionic acid# and L-Phe (4-benzyl)*. The notation * has been utilised for the purpose of the discussion above (r lating to homologous or non-homologous substitution), to indicate the hydrophobic nature of the derivative whereas # has been utilised to indicate the hydrophilic nature of the derivative, #* indicates amphipathic characteristics.

[0120] Variant amino acid sequences may include suitable spacer groups that may be inserted between any two amino acid residues of the sequence including alkyl groups such as methyl, ethyl or propyl groups in addition to amino acid spacers such as glycine or β-alanine residues. A further form of variation, involving the presence of one or more amino acid residues in peptoid form, will be well understood by those skilled in the art. For the avoidance of doubt, “the peptoid form” is used to refer to variant amino acid residues wherein the α-carbon substituent group is on the residue's nitrogen atom rather than the α-carbon. Processes for preparing peptides in the peptoid form are known in the art, for example Simon R J et al., PNAS (1992) 89(20), 9367-9371 and Horwell D C, Trends Biotechnol. (1995) 13(4), 132-134.

[0121] Crystal

[0122] The invention provides a crystal of a retaining glycosyltransferase or a part or fragment thereof, in particular a ligand binding pocket of a glycosyltransferase.

[0123] As used herein, the term “crystal” or “crystalline” means a structure (such as a three dimensional (3D) solid aggregate) in which the plane faces intersect at definite angles and in which there is a regular structure (such as internal structure) of the constituent chemical species. Thus, the term “crystal” can include any one of: a solid physical crystal form such as an experimentally prepared crystal, a crystal structure derivable from the crystal (including secondary and/or tertiary and/or quaternary structural elements), a 2D and/or 3D model based on the crystal structure, a representation thereof such as a schematic representation thereof or a diagrammatic representation thereof, or a data set thereof for a computer. In one aspect, the crystal is usable in X-ray crystallography techniques. Here, the crystals used can withstand exposure to X-ray beams used to produce a diffraction pattern data necessary to solve the X-ray crystallographic structure. A crystalline form of a glycosyltransferase, may be characterized as being capable of diffracting x-rays in a pattern defined by one of the crystal forms depicted in Blundel et al 1976, Protein Crystallography, Academic Press.

[0124] A crystal of the invention comprises an N-terminal α/β pocket with a central core β-sheet characterized by the following: seven strands (β3, β2, β1, β4, β7, β6, β8) all of which are parallel with the exception of β7; the first 100 residues form a nucleotide binding fold composed of four parallel strands sandwiched between two helices (i.e. A and B) on one side and two helices (i.e. C and D) on the other; and the remainder of the core β-sheet is flanked by three α-helices on one side and five on the other.

[0125] The crystal may also be characterized by an antiparallel β-ribbon formed by β5 and β9 lying almost perpendicular to the core β3-sheet, and a substrate binding cleft that lies along the base of the core β3-sheet.

[0126] The C-terminal domain that mediates membrane attachment of a bacterial glycosyltransferase may be predominantly helical. In particular, it may comprise two helices [i.e. helix M and helix N (which is 3₁₀ in nature)] that form a small pedestal that packs perpendicular to the helices of the nucleotide binding motif and to the β-ribbon.

[0127] An illustration of a structure of the invention is shown in FIG. 3.

[0128] In an embodiment, a crystal of a glycosyltransferase of the invention belongs to space group P2₁2₁2₁. The term “space group” refers to the lattice and symmetry of the crystal. In a space group designation the capital letter indicates the lattice type and the other symbols represent symmetry operations that can be carried out on the contents of the asymmetric unit without changing its appearance

[0129] A crystal of the invention may comprise a unit cell having the following unit dimensions: a=37.79 (∀0.05) Å, b=76.05 (∀0.05) Å, c=86.84 (∀0.05) Å. The term “unit cell” refers to the smallest and simplest volume element (i.e. parallelpiped-shaped block) of a crystal that is completely representative of the unit of pattern of the crystal. The unit cell axial lengths are represented by a, b, and c. Those of skill in the art understand that a set of atomic coordinates determined by X-ray crystallography is not without standard error.

[0130] In a preferred embodiment, a crystal of the invention has the structural coordinates of the enzyme as shown in Table 4, Table 5, or Table 6. As used herein, the term “structural coordinates” refers to a set of values that define the position of one or more amino acid residues with reference to a system of axes. A data set of structural coordinates defines the three dimensional structure of a molecule or molecules. The term refers to a data set that defines the three dimensional structure of a molecule or molecules (e.g. Cartesian coordinates, temperature factors, and occupancies). Structural co-ordinates can be slightly modified and still render nearly identical three dimensional structures. A measure of a unique set of structural coordinates is the root-mean-square deviation of the resulting structure. Structural coordinates that render three dimensional structures (in particular a three dimensional structure of a ligand binding pocket) that deviate, from one another by a root-mean-square deviation of less than 5 Å, 4 Å, 3 Å, 2 Å, or 1.5 Å may be viewed by a person of ordinary skill in the art as very similar.

[0131] Variations in structural coordinates may be generated because of mathematical manipulations of the. structural coordinates of a glycosyltransferase described herein. For example, the structural coordinates of Table 4, 5, or 6 may be manipulated by crystallographic permutations of the structural coordinates, fractionalization of the structural coordinates, integer additions or substractions to sets of the structural coordinates, inversion of the structural co-ordinates or any combination of the above.

[0132] Variations in the crystal structure due to mutations, additions, substitutions, and/or deletions of the amino acids, or other changes in any of the components that make up the crystal may also account for modifications in structural coordinates. If such modifications are within an acceptable standard error as compared to the original structural coordinates, the resulting structure may be the same. Therefore, a ligand that bound to a ligand binding pocket of an α1,4-galactosyltransferase would also be expected to bind to another ligand binding pocket whose structural coordinates defined a shape that fell within the acceptable error. Such modified structures of a ligand binding pocket thereof are also within the scope of the invention.

[0133] Various computational analyses may be used to determine whether a ligand or a ligand binding pocket thereof is sufficiently similar to all or parts of a ligand or a ligand binding pocket thereof. Such analyses may be carried out using conventional software applications and methods as described herein.

[0134] A crystal of the invention may also be specifically characterised by the parameters, diffraction statistics and/or refinement statistics set out in Table 2.

[0135] A crystal of the invention may comprise the entire sequence of a retaining galactosyltransferase, preferably from glycosyltransferase family 8 (e.g. see FIG. 2), preferably an α1,4-galactosyltransferase, and most preferably an α-1,4-galactosyltransferase (LgtC) derivable from Neisseria meningitidis. A crystal of the invention may comprise a sequence of a retaining galactosyltransferase with a deletion in or around the C-terminus. Preferably the deletion and/or mutation in the C-terminus is sufficient to facilitate crystallisation of the protein. A crystallized enzyme may not include the portion of a bacterial glycosyltransferase enzyme that attaches to the surface of a bacterial membrane. For example, the C-terminal 25 to 50 amino acid residues may be deleted from an α-1,4-galactosyltransferase (LgtC) derivable from Neisseria meningitidis.

[0136] Ligand-Binding Pocket

[0137] In an embodiment the invention provides a crystal comprising a ligand binding pocket.

[0138] “Ligand binding pocket” or “LBP” refers to a region of a molecule or molecular complex that as a result of its shape, favourably associates with a ligand or a part thereof. For example, it may be a region of a glycosyltransferase that is responsible for binding a ligand including a donor molecule, an acceptor molecule and/or a sugar during transfer (e.g. active site binding pocket). With reference to the models and structures of the invention, residues in a ligand binding pocket may be defined by their spatial proximity to a ligand in a model or structure.

[0139] A “ligand” refers to a compound or entity that associates with a ligand binding pocket, including substrates such as acceptor molecules or analogues or parts thereof, donor molecules or analogues or parts thereof A ligand may be designed rationally by using a model according to the present invention. A ligand may be a modulator of a glycosyltransferase including an inhibitor.

[0140] A “donor molecule” or “sugar nucleotide donor” refers to a molecule capable of donating a sugar to an acceptor molecule, via the action of a glycosyltransferase enzyme. The donor molecule may be di- or poly-saccharides, sugar 1-phosphates, or, most commonly, nucleotide diphosphosugars (NDP-sugars), or nucleotide phosphosugars. In a preferred embodiment, the donor molecule is UDP-galactose, UDP glucose, UDP mannose, UDP-N-acetylglucosamine, UDP-N-acetylgalactosamine, UDP-N-acetymannosamine, UDP-glucuronic acid, UDP-galacturonic acid, UDP-fucose, UDP-xylose, UDP-rhamnose, and ADP, GDP and TDP derivatives thereof, and CMP sialic acid.

[0141] An acceptor molecule is capable of accepting a sugar from a donor molecule, via the action of a glycosyltransferase enzyme. It may, for example, comprise a terminal sugar residue for transfer purposes. The acceptor molecule or aglycone can be, for example, a lipid, a protein, a heterocyclic compound, an antibiotic, a peptide, an amino acid, an aromatic or aliphatic alcohol or thiol or another carbohydrate residue. In a preferred embodiment, the donor molecule is or comprises a terminal lactose.

[0142] An analogue of a donor or acceptor molecule is one which mimics the donor or acceptor molecule, binding in the LBP, but which is incapable (or has a significantly reduced capacity) to take part in the transfer reaction. For example, UDP-Gal can act as a donor sugar for a galactosyltransferase. UDP-2Fgal, on the other hand, acts as a donor sugar analogue. The fluorine at the 2-position destabilises the transition state for the transfer reaction, so that effectively no transfer occurs. Similarly, UDPGlcNAc can act as a donor sugar for GnT1 and the methylene phosphonate analogue can act as a donor sugar analogue. By the same token, a terminal lactose can act as an acceptor sugar for a α1,4 galactosyltransferase. 4-deoxylactose is non reactive and is an example of an acceptor molecule analogue.

[0143] The term “ligand binding pocket” (LBP) includes a homologue of the ligand binding pocket or a portion thereof. As used herein, the term “homologue” in reference to a ligand binding pocket refers to ligand binding pocket or a portion thereof which may have deletions, insertions or substitutions of amino acid residues as long as the binding specificity of the molecule is retained. In this regard, deliberate amino acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues as long as the binding specificity of the ligand binding pocket is retained.

[0144] As used herein, the term “portion thereof” means the structural co-ordinates corresponding to a sufficient number of amino acid residues of the glycosyltransferase LBP (or homologues thereof) that are capable of associating or interacting with a ligand. This term includes glycosyltransferase ligand binding pocket amino acid residues having amino acid residues from about 4 Å to about 5 Å of an associated ligand or part thereof. Thus, for example, the structural co-ordinates provided in a crystal structure may contain a subset of the amino acid residues in the LBP which may be useful in the modelling and design of compounds that bind to the LBP.

[0145] A crystal of the invention may comprise a ligand binding pocket and at least part of the pocket which may be involved in attaching the enzyme to the bacterial membrane. Preferably the crystal comprises the entire sequence of the enzyme, optionally with a deletion in or around the C-terminus. Preferably the deletion and/or mutation in the C-terminus is sufficient to facilitate crystallisation of the protein.

[0146] A ligand-binding pocket may comprise an active site binding pocket of a glycosyltransferase. The active site binding pocket refers to the region of a glycosyltransferase where the transfer of a sugar from the donor molecule to the acceptor occurs. In accordance with one aspect, the invention contemplates a crystal of an active site binding pocket of a retaining glycosyltransferase comprising a core β-sheet containing 7 strands (β3, β2, β1, β4, β6, β8 in FIG. 3) all of which are parallel with the exception of β7; the core β-sheet further characterized by a nucleotide binding motif composed of four parallel strands sandwiched between helices A and B on one side and helices C and D on the other as shown in FIG. 3. A polypeptide comprising an active site binding pocket with the shape and structure of an active site binding pocket described herein is also within the scope of the invention.

[0147] The ligand binding pocket may comprise a pocket of a glycosyltransferase structure described herein that is capable of associating with a donor molecule, preferably a nucleotide or portion thereof. A ligand binding pocket may comprise the amino acid residues at the C-terminus of β1 and the N-terminus of helix A of a glycosyltransferase structure as described herein, that are capable of associating with a nucleotide of a donor molecule as described herein. In particular, a ligand-binding pocket may comprise one or both of the loops that associate with a donor molecule or analogue. Such a ligand binding pocket may comprise a loop comprising residues 75-80 and/or a loop comprising residues 246-251 of a glycosyltransferase described herein or a homologue thereof.

[0148] A ligand binding pocket may comprise a cleft at the C-terminal end of a glycosyltransferase β-sheet structure as described herein that is capable of associating with a uridine diphosphate. The ligand binding pocket may comprise a conserved Tyr 11 (Phe in E. coli and Salmonella) of a glycosyltransferase structure as described herein that is capable of stacking with a uracil base.

[0149] When UDP-Gal is capable of acting as a donor molecule for the glycosyltransferase enzyme, preferably the ligand binding pocket may comprise at least one of the residues involved in binding to the UDP portion of UDP-Gal, namely: Tyr 11, Asn 10, Asp 8, Ala 6, Ile 104, Lys 250, Gly 247 and His 78 or a homologue thereof.

[0150] When UDP-Gal is capable of acting as a donor molecule for the glycosyltransferase enzyme, preferably the ligand binding pocket may comprise at least one of the residues involved in binding to the UDP portion of UDP-Gal, namely: Asp 8, Asn 10, Ala 6, Ile 104, Lys 250, Gly 247, and His 78 or a homologue thereof.

[0151] Alternatively, or more preferably in addition, the ligand binding pocket may comprise at least one of the residues involved in shielding the reactive center C1′ atom from water, namely: Ile 76, Asp 103, Asp 153, Ala 154, Gly 155, Tyr 186, Gln 189, His 244, Cys 246 and Gly 247; or a homologue thereof.

[0152] Based on the crystal of LgtC herein, Gln 189 may act as the nucleophile during the transfer reaction. Hence, in an embodiment a crystal of the invention comprises Gln 189 or a homologue thereof. Preferably, the Glnl89 is oriented through hydrogen bonds to both sugar (donation of a hydrogen bond from Nεl to O6 of lactose) and conserved protein side chains (acceptance of a hydrogen bond from the side chain Nε2 of Asn153).

[0153] Alternatively, or more preferably in addition, the ligand binding pocket may comprise at least one of the residues involved in binding to a sugar moiety of a donor molecule such as the galactosyl moiety of UDP-Gal, namely: Asp103, Arg 86, Asp 188, and optionally one or more of Asn 153, Val 79, Thr 83, Gln 187 and Gln 189 or a homologue thereof.

[0154] When lactose is capable of acting as an acceptor molecule for the glycosyltransferase. enzyme, the ligand binding pocket may comprise at least one of the residues involved in binding to lactose, namely: Asp130, Gln 189, Val 76, His 78, Tyr 186, Cys 246, Gly 247, Phe 132, Pro 211, Pro 248, Thr 212 and Cys 246; or a homologue thereof.

[0155] With reference to a crystal of the present invention, residues in the LBP may be defined by their spatial proximity to a ligand in the crystal structure. For example, such may be defined by their proximity to a donor and/or an acceptor molecule.

[0156] A ligand binding pocket may comprise one or more of the residues involved in co-ordination of a Mn²⁺ ion, namely: His 244, Asp 103 and Asp 105; or a homologue thereof.

[0157] Preferably a LBP comprises at least one DXD motif. A “DXD” sequence motif is common to a wide range of glycosyltransferases, both in prokaryotes and eukaryotes, even though they may not share other sequence similarities. (Campbell et al., 1997 Biochemical Journal 326, 929-939, Breton et al., 1998 Journal of Biochemistry 123, 1000-1009 and Kapitonov and Yu, 1999 Glycobiology 9, 961-978). This motif has been proposed to be involved in the coordination of a divalent cation in the binding of the nucleotide sugar (Busch et al., 1998 The Journal of Biological Chemistry 273, 19566-19572). A number of mutagenesis studies have been carried out in various species on the conserved aspartate residues in the DXD sequence and all have found that enzymatic activity is completely abolished upon removal of the carboxylate (Shibayama et al., 1998 Journal of Bacteriology 180, 5313-5318, Wiggins and Munro, 1998 Proc. Natl. Acad Sci. USA 95, 7945-7950, Busch et al., 1998 (as above) and Hagen et al., 1999 The Journal of Biological Chemistry 274, 6797-6803).

[0158] A ligand binding pocket may comprise one or more of the amino acid residues for a glycosyltransferase structure of the invention identified by atomic contacts on the enzyme for atomic interactions numbers 1 through 17 shown in Table 3.

[0159] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase that associates with a diphosphate of a sugar nucleotide donor molecule is provided comprising one or both of the enzyme atomic contacts of atomic interactions 6 and 7 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the diphosphate group, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket is defined by the atoms of the enzyme atomic contacts of atomic interactions 6 and/or 7 having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0160] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase that associates with a heterocyclic amine base (preferably uracil) of a sugar nucleotide donor molecule is provided comprising one, two, or three of the enzyme atomic contacts of atomic interactions 1,2, and 3 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the heterocyclic amine base, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket is defined by the atoms of the enzyme atomic contacts of atomic interactions 1, 2, and/or 3 having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0161] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase that associates with a sugar of the nucleotide (preferably ribose) of a sugar nucleotide donor molecule is provided comprising one or both of the enzyme atomic contacts of atomic interactions 4 and 5 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the sugar, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket is defined by the atoms of the enzyme atomic contacts of atomic interactions 4 and/or 5 having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0162] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase that associates with a sugar to be transferred (e.g. Gal) of a sugar nucleotide donor molecule is provided comprising one, two, or three enzyme atomic contacts of atomic interactions 8, 9, and 10 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the selected sugar, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket is defined by the atoms of the enzyme atomic contacts of atomic interactions 8, 9, and/or 10 having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0163] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase that associates with a nucleotide (preferably UDP) of a sugar nucleotide donor molecule is provided comprising one, two, three, four, five, six, or seven enzyme atomic contacts of atomic interactions 1 through 7 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the nucleotide, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of a binding pocket is defined by the atoms of one, two, three, four, five, six, or seven enzyme atomic contacts of atomic interactions 1 through 7 having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0164] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase that associates with a sugar nucleotide donor molecule (e.g. UDP-Gal) is provided comprising one, two, three, four, five, six, seven, eight, nine, or ten enzyme atomic contacts of atomic interactions 1 through 10 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the sugar nucleotide donor molecule, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket is defined by the atoms of one, two, three, four, five, six, seven, eight, nine, or ten enzyme atomic contacts of atomic interactions 1 through 10 having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0165] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase that associates with an acceptor molecule (e.g. acceptor with a terminal lactose) is provided comprising one two, three, four, five, or six enzyme atomic contacts of atomic interactions 12 through 17 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the acceptor molecule, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket is defined by the atoms of one, two, three, four, five, or six enzyme atomic contacts of atomic interactions 12 through 17 having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0166] Complexes

[0167] A crystal of the invention includes a crystalline glycosyltransferase or part thereof (e.g. ligand binding pocket) in association with one or more moieties, including heavy-metal atoms i.e. a derivative crystal, a metal cofactor, or one or more ligands or molecules i.e. a co-crystal.

[0168] The term “associate”, “association” or “associating” refers to a condition of proximity between a moiety (i.e. chemical entity or compound or portions or fragments thereof), and a glycosyltransferase, or parts or fragments thereof (e.g. ligand binding pockets). The association may be non-covalent i.e. where the juxtaposition is energetically favoured by for example, hydrogen-bonding, van der Waals, or electrostatic or hydrophobic interactions, or it may be covalent.

[0169] The term “heavy-metal atoms” refers to an atom that can be used to solve an x-ray crystallography phase problem, including but not limited to a transition element, a lanthanide metal, or an actinide metal. Lanthanide metals include elements with atomic numbers between 57 and 71, inclusive. Actinide metals include elements with atomic numbers between 89 and 103, inclusive.

[0170] Multiwavelength anomalous diffraction (MAD) phasing may be used to solve protein structures using selenomethionyl (SeMet) proteins. Therefore, a complex of the invention may comprise a crystalline glycosyltransferase or part thereof (e.g. ligand binding pocket) with selenium associated with the methionine residues of the protein.

[0171] In an embodiment of the invention, a ligand binding pocket is in association with a metal cofactor in the crystal. A “metal cofactor” refers to a metal required for glycosyltransferase activity and/or stability. For example, the metal cofactor may be manganese, and other similar atoms or metals. Different glycosyltransferases may require different cofactors, for example Mn²⁺, Mg²⁺, Co²⁺, Zn²⁺, Fe²⁺, and Ca²⁺. In a preferred embodiment the LBP is in association with manganese.

[0172] A ligand binding pocket in a complex with a cofactor preferably comprises one or more of the residues involved in co-ordination of a Mn2+ ion, namely: His 244, Asp 103 and Asp 105; or a homologue thereof. Preferably the LBP comprises at least one DXD motif.

[0173] A crystal may comprise a complex between a ligand-binding pocket and one or more ligands or molecules. In other words the ligand binding pocket may be associated with one or more ligands or molecules in the crystal. The ligand may be any compound which is capable of stably and specifically associating with the ligand binding pocket A ligand may, for example, be a substrate such as a donor or an acceptor molecule or analogue thereof, and/or the ligand may be a modulator of the glycosyltransferase.

[0174] Therefore, the present invention also provides:

[0175] (a) a crystal comprising a ligand binding pocket of a glycosyltransferase and a donor molecule or analogue thereof;

[0176] (b) a crystal comprising a ligand binding pocket of a glycosyltransferase and an acceptor molecule or analogue thereof;

[0177] (c) a crystal comprising a ligand binding pocket of a glycosyltransferase and a donor molecule or analogue thereof, and an acceptor molecule thereof .

[0178] A complex may comprise one or more of the atomic interactions identified in Table 3. A structure of a complex of the invention may be defined by selected atomic interactions, preferably the atomic interactions as defined in Table 3.

[0179] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase in association with a diphosphate of a sugar nucleotide donor molecule is provided comprising one or both of atomic interactions 6 and 7 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the diphosphate group, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of such a complex is defined by the atoms of the atomic contacts of the atomic interactions having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0180] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase in association with a heterocyclic amine base (preferably uracil) of a sugar nucleotide donor molecule is provided comprising one, two, or three of atomic interactions 1, 2, and 3 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the heterocyclic amine base, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of a such a complex is defined by the atoms of the atomic contacts of the atomic interactions having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0181] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase in association with a sugar of the nucleotide (preferably ribose) of a sugar nucleotide donor molecule is provided comprising one or both of atomic interactions 4 and. 5 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the sugar, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of such a complex is defined by the atoms of the atomic contacts of the atomic interactions having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0182] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase in association with a sugar to be transferred (e.g. Gal) of a sugar nucleotide donor molecule is provided comprising one, two, or three of atomic interactions 8, 9, and 10 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the selected sugar, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of such a complex is defined by the atoms of the atomic contacts of the atomic interactions having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0183] In an embodiment of the invention, a crystal of a ligand binding pocket or secondary, tertiary, and/or quanternary structure of a glycosyltransferase in association with a nucleotide (preferably UDP) of a sugar nucleotide donor molecule is provided comprising one, two, three, four, five, six, or seven of atomic interactions 1 through 7 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the nucleotide, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably, a crystal or secondary, tertiary, and/or quanternary structure of such a complex is defined by the atoms of the atomic contacts of the atomic interactions having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0184] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase in association with a sugar nucleotide donor molecule (e.g. UDP-Gal) is provided comprising one, two, three, four, five, six, seven, eight, nine, or ten of atomic interactions 1 through 10 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the sugar nucleotide donor molecule, and an atomic contact (more preferably, a specific amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably a crystal or secondary, tertiary, and/or quanternary structure of such a complex is defined by the atoms of the atomic contacts of atomic interactions having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0185] In an embodiment of the invention, a crystal or secondary, tertiary, and/or quanternary structure of a ligand binding pocket of a glycosyltransferase in association with an acceptor molecule (e.g. acceptor with a terminal lactose) is provided comprising one two, three, four, five, or six of atomic interactions 12 through 17 identified in Table 3, each atomic interaction defined therein by an atomic contact (more preferably, a specific atom where indicated) on the acceptor molecule, and an atomic contact (more preferably, a specific. amino acid residue where indicated) on the glycosyltransferase (i.e. enzyme atomic contact). Preferably a crystal or secondary, tertiary, and/or quanternary structure of such a complex is defined by the atoms of the atomic contacts of the atomic interactions having the structural coordinates for the atoms listed in Table 4, 5, or 6.

[0186] In an embodiment a crystal of the invention comprises a ligand binding pocket of a galactosyltransferase in association with a donor molecule, such as UDP-2Fgal and/or an acceptor molecule such as 4-deoxylactose or lactose. These complexes may have the structural coordinates shown in Table 4, 5, or 6.

[0187] A crystal of the invention may enable the determination of structural data for the donor molecule or acceptor molecule. In order to be able to derive structural data for the donor/acceptor molecule, it is necessary for the molecule to have sufficiently strong electron density to enable a model of the molecule to be built using standard techniques. For example, there should be sufficient electron density to allow a model to be built using XTALVIEW (McRee 1992 J. Mol. Graphics. 10 44-46).

[0188] Method of Making a Crystal

[0189] The present invention also provides a method of making a crystal according to the invention. The crystal may be formed from an aqueous solution comprising a purified polypeptide comprising a glycosyltransferase or part or fragment thereof (e.g. a catalytic portion, ligand binding pocket). A method may utilize a purified polypeptide comprising a glycosyltransferase ligand binding pocket to form a crystal

[0190] The term “purified” in reference to a polypeptide, does not require absolute purity such as a homogenous preparation rather it represents an indication that the polypeptide is relatively purer than in the natural environment Generally, a purified polypeptide is substantially free of other proteins, lipids, carbohydrates, or other materials with which it is naturally associated, preferably at a functionally significant level for example at least 85% pure, more preferably at least 95% pure, most preferably at least 99% pure. A skilled artisan can purify a polypeptide comprising a glycosyltransferase using standard techniques for protein purification. A substantially pure polypeptide comprising a glycosyltransferase will yield a single major band on a non-reducing polyacrylamide gel. The purity of the glycosyltransferase can also be determined by amino-terminal amino acid sequence analysis.

[0191] A polypeptide used in the method may be chemically synthesized in whole or in part using techniques that are well-known in the art. Alternatively, methods are well known to the skilled artisan to construct expression vectors containing the native or mutated glycosyltransferase coding sequence and appropriate transcriptional/translational control signals. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo recombination/genetic recombination. See for example the techniques described in Sambrook et al. Molecular Cloning: A Laboratory Manual, 2nd Edition, Cold Spring Harbor Laboratory press (1989)), and other laboratory textbooks. (See also Sarker et al, Glycoconjugate 1. 7:380, 1990; Sarker et al, Proc. Natl. Acad, Sci. USA 88:234-238, 1991, Sarker et al, Glycoconjugate J. 11: 204-209, 1994; Hull et al, Biochem Biophys Res Commun 176:608, 1991 and Pownall et al, Genomics 12:699-704, 1992).

[0192] Preferably the polypeptide comprises a glycosyltransferase enzyme or part thereof having a mutation in the part of the enzyme which is involved in attachment to bacterial membranes. In a preferred embodiment the polypeptide comprises a glycosyltransferase enzyme or part thereof having a deletion at or around the C-terminus. In particular, such a deletion may serve to reduce the proportion of basic and/or hydrophobic and/or aromatic residues. The polypeptide may, for example, be missing the C-terminal 25 residues.

[0193] Preferably the polypeptide comprises one or more mutations which serve to reduce or eliminate aggregation of the polypeptide. For example, the polypeptide may comprise one or more mutations (e.g. substitutions or deletions) of cysteine residues.

[0194] Crystals may be grown from an aqueous solution containing the purified glycosyltransferase polypeptide by a variety of conventional processes. These processes include batch, liquid, bridge, dialysis, vapor diffusion, and hanging drop methods. (See for example, McPherson, 1982 John Wiley, New York; McPherson, 1990, Eur. J. Biochem. 189: 1-23; Webber. 1991, Adv. Protein Chem. 41:1-36). Generally, the native crystals of the invention are grown by adding precipitants to the concentrated solution of the glycosyltransferase polypeptide. The precipitants are added at a concentration just below that necessary to precipitate the protein. Water is removed by controlled evaporation to produce precipitating conditions, which are maintained until crystal growth ceases.

[0195] Derivative crystals of the invention can be obtained by soaking native crystals in a solution containing salts of heavy metal atoms. A complex of the invention can be obtained by soaking a native crystal in a solution containing a compound that binds the polypeptide, or they can be obtained by co-crystallizing the polypeptide in the presence of one or more compounds. In order to obtain co-crystals with a compound which binds deep within the tertiary structure of the polypeptide (for example UDP-2FGal is almost entirely buried by LgtC when bound) it is necessary to use the second method.

[0196] In a preferred embodiment, the polypeptide is cocrystallised with a compound which stabilises the polypeptide. For example, the compound may stabilise one or both of the loops made up of residues 75-80 and 246-251. In a highly preferred embodiment the polypeptide is cocrystallised with an inert analogue of the sugar donor, for example UDP 2-deoxy-2-fluorogalactose.

[0197] Once the crystal is grown it can be placed in a glass capillary tube and mounted onto a holding device connected to an X-ray generator and an X-ray detection device. Collection of X-ray diffraction patterns are well documented by those skilled in the art (See for example, Ducruix and Geige, 1992, IRL Press, Oxford, England). A beam of X-rays enter the crystal and diffract from the crystal. An X-ray detection device can be utilized to record the diffraction patterns emanating from the crystal. Suitable devices include the Marr 345 imaging plate detector system with an RU200 rotating anode generator.

[0198] Methods for obtaining the three dimensional structure of the crystalline form of a molecule or complex are described herein and known to those skilled in the art (see Ducruix and Geige 1992, IRL Press, Oxford, England). Generally, the x-ray crystal structure is given by the diffraction patterns. Each diffraction pattern reflection is characterized as a vector and the data collected at this stage determines the amplitude of each vector. The phases of the vectors may be determined by the isomorphous replacement method where heavy atoms soaked into the crystal are used as reference points in the X-ray analysis (see for example, Otwinowski, 1991, Daresbury, United Kingdom, 80-86). The phases of the vectors may also be determined by molecular replacement (see for example, Naraza, 1994, Proteins 11:281-296). The amplitudes and phases of vectors from the crystalline form of a glycosyltransferase determined in accordance with these methods can be used to analyze other related crystalline polypeptides.

[0199] The unit cell dimensions and symmetry, and vector amplitude and phase information can be used in a Fourier transform function to calculate the electron density in the unit cell i.e. to generate an experimental electron density map. This may be accomplished using the PHASES package (Furey, 1990). Amino acid sequence structures are fit to the experimental electron density map (i.e. model building) using computer programs (e.g. Jones, T A. et al, Acta Crystallogr A47, 100-119, 1991). This structure can also be used to calculate a theoretical electron density map. The theoretical and experimental electron density maps can be compared and the agreement between the maps can be described by a parameter referred to as R-factor. A high degree of overlap in the maps is represented by a low value R-factor. The R-factor can be minimized by using computer programs that refine the structure to achieve agreement between the theoretical and observed electron density map. For example, the XPLOR program, developed by Brunger (1992, Nature 355:472-475) can be used for model refinement.

[0200] A three dimensional structure of the molecule or complex may be described by atoms that fit the theoretical electron density characterized by a minimum R value. Files can be created for the structure that defines each atom by co-ordinates in three dimensions.

[0201] Model

[0202] A crystal structure of the present invention may be used to make a model of the glycosyltransferase or a part thereof, (e.g. a ligand-binding pocket). A model may, for example, be a structural model or a computer model. A model may represent the secondary, tertiary and/or quaternary structure of the glycosyltransferase. The model itself may be in two or three dimensions. It is possible for a computer model to be in three dimensions despite the constraints imposed by a conventional computer screen, if it is possible to scroll along at least a pair of axes, causing “rotation” of the image.

[0203] As used herein, the term “modelling” includes the quantitative and qualitative analysis of molecular structure and/or function based on atomic structural information and interaction models. The term “modelling” includes conventional numeric-based molecular dynamic and energy minimization models, interactive computer graphic models, modified molecular mechanics models, distance geometry and other structure-based constraint models.

[0204] Preferably, modelling is performed using a computer and may be further optimized using known methods. This is called modelling optimisation.

[0205] The three dimensional structure of a new crystal may be modelled using molecular replacement The term “molecular replacement” refers to a method that involves generating a preliminary model of a molecule or complex whose structural co-ordinates are unknown, by orienting and positioning a molecule whose structural co-ordinates are known within the unit cell of the unknown crystal, so as best to account for the observed diffraction pattern of the unknown crystal. Phases can then be calculated from this model and combined with the observed amplitudes to give an approximate Fourier synthesis of the structure whose coordinates are unknown. This, in turn, can be subject to any of the several forms of refinement to provide a final, accurate structure of the unknown crystal. Lattman, E., “Use of the Rotation and Translation Functions”, in Methods in Enzymology, 115, pp. 55-77 (1985); M. G. Rossmann, ed., “The Molecular Replacement Method”, Int. Sci. Rev. Ser., No. 13, Gordon & Breach, New York, (1972).

[0206] Commonly used computer software packages for molecular replacement are X-PLOR (Brunger 1992, Nature 355: 472-475), AMORE (Navaza, 1994, Acta Crystallogr. A50:157-163), the CCP4 package (Collaborative Computational Project, Number 4, “The CCP4 Suite: Programs for Protein Crystallography”, Acta Cryst., Vol. D50, pp. 760-763, 1994), the MERLOT package (P. M. D. Fitzgerald, J. Appl. Cryst., Vol. 21, pp. 273-278, 1988) and XTALVIEW (McCree et al (1992) J. Mol. Graphics 10: 44-46. It is preferable that the resulting structure not exhibit a root-mean-square deviation of more than 3 Å.

[0207] Molecular replacement computer programs generally involve the following steps: (1) determining the number of molecules in the unit cell and defining the angles between them (self rotation function); (2) rotating the known structure against diffraction data to define the orientation of the molecules in the unit cell (rotation function); (3) translating the known structure in three dimensions to correctly position the molecules in the unit cell (translation function); (4) determining the phases of the X-ray diffraction data and calculating an R-factor calculated from the reference data set and from the new data wherein an R-factor between 30-50% indicates that the orientations of the atoms in the unit cell have been reasonably determined by the method; and (5) optionally, decreasing the R-factor to about 20% by refining the new electron density map using iterative refinement techniques known to those skilled in the art (refinement).

[0208] The quality of the model may be analysed using a program such as PROCHECK or 3D-Profiler [Laskowski et al 1993 J. Appl. Cryst. 26:283-291; Luthy R. et al, Nature 356: 83-85, 1992; and Bowie, J. U. et al Science 253: 164-170, 1991]. Once any irregularities have been resolved, the entire structure may be further refined.

[0209] Other molecular modelling techniques may also be employed in accordance with this invention. See, e.g., Cohen, N. C. et al, “Molecular Modelling Software and Methods for Medicinal Chemistry”, J. Med. Chem., 33, pp. 883-894 (1990). See also, Navia, M. A. and M. A. Murcko, “The Use of Structural Information in Drug Design”, Current Opinions in Structural Biology, 2, pp. 202-210 (1992).

[0210] Computer format of Crystals/Models

[0211] Information derivable from the crystal of the present invention (for example the structural coordinates) and/or the model of the present invention may be provided in a computer-readable format.

[0212] Therefore, the invention provides a computer readable medium or a machine readable storage medium which comprises the structural co-ordinates of a retaining glycosyltransferase including all or any parts of the glycosyltransferase (e.g ligand-binding pockets), one or more ligands including substrates, for example, acceptor molecules including portions thereof, or donor molecules including portions thereof. Such storage medium or storage medium encoded with these data are capable of displaying on a computer screen or similar viewing device, a three-dimensional graphical representation of a molecule or molecular complex which comprises the enzyme or ligand binding pockets or similarly shaped homologous enzymes or ligand binding pockets. Thus, the invention also provides computerized representations of a crystal of the invention, including any electronic, magnetic, or electromagnetic storage forms of the data needed to define the structures such that the data will be computer readable for purposes of display and/or manipulation.

[0213] In an aspect the invention provides a computer for producing a three-dimensional representation of a molecule or molecular complex, wherein said molecule or molecular complex comprises a retaining glycosyltransferase or ligand binding pocket thereof defined by structural coordinates of retaining glycosyltransferase amino acids or a ligand binding pocket thereof, or comprises structural coordinates of atoms of a ligand in particular a substrate (e.g. an acceptor or donor molecule), or a three-dimensional representation of a homologue of said molecule or molecular complex, wherein said computer comprises:

[0214] (a) a machine-readable data storage medium comprising a data storage material encoded with machine readable data wherein said data comprises the structural coordinates of a retaining glycosyltransferase amino acids according to Table 4, 5, or 6 or a ligand binding pocket thereof, or an acceptor or donor molecule according to Table 4, 5, or 6;

[0215] (b) a working memory for storing instructions for processing said machine-readable data;

[0216] (c) a central-processing unit coupled to said working memory and to said machine-readable data storage medium for processing said machine readable data into said three-dimensional representation; and

[0217] (d) a display coupled to said central-processing unit for displaying said three-dimensional representation.

[0218] A homologue may comprise a glycosyltransferase or ligand binding pocket thereof, or acceptor or donor molecule that has a root mean square deviation from the backbone atoms of not more than 1.5 angstroms.

[0219] The invention also provides a computer for determining at least a portion of the structural coordinates corresponding to an X-ray diffraction pattern of a molecule or molecular complex wherein said computer comprises:

[0220] (a) a machine-readable data storage medium comprising a data storage material encoded with machine readable data wherein said data comprises the structural coordinates according to Table 4, 5, or 6;

[0221] (b) a machine-readable data storage medium comprising a data storage material encoded with machine readable data wherein said data comprises an X-ray diffraction pattern of said molecule or molecular complex;

[0222] (c) a working memory for storing instructions for processing said machine-readable data of (a) and (b);

[0223] (d) a central-processing unit coupled to said working memory and to said machine-readable data storage medium of (a) and (b) for performing a Fourier transform of the machine readable data of (a) and for processing said machine readable data of (b) into structural coordinates; and

[0224] (e) a display coupled to said central-processing unit for displaying said structural coordinates of said molecule or molecular complex.

[0225] The invention also contemplates a computer programmed with a model of a ligand binding pocket according to the invention; a machine-readable data-storage medium on which has been stored in machine-readable form a model of a ligand binding pocket of a glycosyltransferase; and the use of a model as input to a computer programmed for drug design and/or database searching and/or molecular graphic imaging in order to identify new ligands or modulators for glycosyltransferases.

[0226] Structural Determinations

[0227] The present invention also provides a method for determining the secondary and/or tertiary structures of a polypeptide by using a crystal, or a model according to the present invention. The polypeptide may be any polypeptide for which the secondary and or tertiary structure is uncharacterised or incompletely characterised. In a preferred embodiment the polypeptide shares (or is predicted to share) some structural or functional homology to the glycosyltransferase of the crystal. For example, the polypeptide may show a degree of structural homology over some or all parts of the primary amino acid sequence. For example the polypeptide may have one or more pockets which shows homology with a glycosyltransferase pocket (Kapitonov and Yu (1999) Glycobiology 9(10): 961-978).

[0228] Two polypeptides are considered to show substantial structural homology when the two peptide sequences, when optimally aligned (such as by the programs GAP or BESTFIT using default gap) share at least 40%, 50%, 60%, 65%, 70%, 75%, 80%, or 85% sequence identity, preferably at least 90 percent sequence identity, more preferably at least 95 percent sequence identity or more. Preferably, residue positions which are not identical differ by conservative amino acid substitutions. For example, the substitution of amino acids having similar chemical properties such as charge or polarity are not likely to affect the properties of a protein. Examples include glutamine for asparagine or glutamic acid for aspartic acid.

[0229] The polypeptide may be a glycosyltransferase with a different specificity for a ligand or portion thereof including a sugar residue, donor molecule or acceptor molecule. The polypeptide may be a glycosyltransferase which requires a different metal cofactor. Alternatively (or in addition) the polypeptide may be a glycosyltransferase enzyme from a different species.

[0230] The polypeptide may be a mutant of the wild-type glycosyltransferase. A mutant may arise naturally, or may be made artificially (for example using molecular biology techniques). The mutant may also not be “made” at all in the conventional sense, but merely tested theoretically using the model of the present invention. A mutant may or may not be functional.

[0231] Thus, using a model of the present invention, the effect of a particular mutation on the overall two and/or three dimensional structure of the glycosyltransferase and/or the interaction between the enzyme and a ligand can be investigated.

[0232] Alternatively, the polypeptide may perform an analogous function or be suspected to show a similar catalytic mechanism to the glycosyltransferase enzyme. For example the polypeptide may remove, transport, or add on a sugar residue. If the glycosyltransferase of the crystal is a retaining glycosyltransferase, the polypeptide under investigation may be known or suspected to function via a double-displacement mechanism.

[0233] The polypeptide may also be the same as the polypeptide of the crystal, but in association with a different ligand (for example, donor molecule, acceptor molecule analogue, modulator or inhibitor) or cofactor. In this way it is possible to investigate the effect of altering the ligand or compound with which the polypeptide is associated on the structure of the LBP.

[0234] Secondary or tertiary structure may be determined by applying the structural coordinates of the crystal or model of the present invention to other data such as an amino acid sequence, X-ray crystallographic diffraction data, or nuclear magnetic resonance (NMR) data. Homology modeling, molecular replacement, and nuclear magnetic resonance methods using these other data sets are described below.

[0235] Homology modeling (also known as comparative modeling or knowledge-based modeling) methods develop a three dimensional model from a polypeptide sequence based on the structures of known proteins (i.e. the glycosyltransferase of the crystal). The method utilizes a computer model of the crystal of the present invention (the “known structure”), a computer representation of the amino acid sequence of the polypeptide with an unknown structure, and standard computer representations of the structures of amino acids. The method in particular comprises the steps of; (a) identifying structurally conserved and variable regions in the known structure; (b) aligning the amino acid sequences of the known structure and unknown structure (c) generating coordinates of main chain atoms and side chain atoms in structurally conserved and variable regions of the unknown structure based on the coordinates of the known structure thereby obtaining a homology model; and (d) refining the homology model to obtain a three dimensional structure for the unknown structure. This method is well known to those skilled in the art (Greer, 1985, Science 228, 1055; Bundell et al 1988, Eur. J. Biochem. 172, 513; Knighton et al., 1992, Science 258:130-135, http://biochem.vt.edu/courses/modeling/homology.htn). Computer programs that can be used in homology modelling are Quanta and the Homology module in the Insight II modelling package distributed by Molecular Simulations Inc, or MODELLER (Rockefeller University, www.iucr.ac.uk/sinris-top/logical/prg-modeller.html).

[0236] In step (a) of the homology modelling method, the known glycosyltransferase structure is examined to identify the structurally conserved regions (SCRs) from which an average structure, or framework, can be constructed for these regions of the protein. Variable regions (VRs), in which known structures may differ in conformation, also must be identified. SCRs generally correspond to the elements of secondary structure, such as alpha-helices and beta-sheets, and to ligand- and substrate-binding sites (e.g. acceptor and donor binding sites). The VRs usually lie on the surface of the proteins and form the loops where the main chain turns.

[0237] Many methods are available for sequence alignment of known structures and unknown structures. Sequence alignments generally are based on the dynamic programming algorithm of Needleman and Wunsch [J. Mol. Biol. 48: 442453, 1970]. Current methods include FASTA, Smith-Waterman, and BLASTP, with the BLASTP method differing from the other two in not allowing gaps. Scoring of alignments typically involves construction of a 20×20 matrix in which identical amino acids and those of similar character (i.e., conservative substitutions) may be scored higher than those of different character. Substitution schemes which may be used to score alignments include the scoring matrices PAM (Dayhoff et al., Meth. Enzymol. 91: 524-545, 1983), and BLOSUM (Henilcoff and Henikoff, Proc. Nat. Acad. Sci. USA 89: 10915-10919, 1992), and the matrices based on alignments derived from three-dimensional structures including that of Johnson and Overington (JO matrices) (J. Mol. Biol. 233: 716-738, 1993).

[0238] Alignment based solely on sequence may be used; however, other structural features also may be taken into account. In Quanta, multiple sequence alignment algorithms are available that may be used when aligning a sequence of the unknown with the known structures. Four scoring systems (i.e. sequence homology, secondary structure homology, residue accessibility homology, CA-CA distance homology) are available, each of which may be evaluated during an alignment so that relative statistical weights may be assigned.

[0239] When generating co-ordinates for the unknown structure, main chain atoms and side chain atoms, both in SCRs and VRs need to be modelled. A variety of approaches known to those skilled in the art may be used to assign coordinates to the unknown. In particular, the coordinates of the main chain atoms of SCRs will be transferred to the unknown structure. VRs correspond most often to the loops on the surface of the polypeptide and if a loop in the known structure is a good model for the unknown, then the main chain coordinates of the known structure may be copied. Side chain coordinates of SCRs and VRs are copied if the residue type in the unknown is identical to or very similar to that in the known structure. For other side chain coordinates, a side chain rotamer library may be used to define the side chain coordinates. When a good model for a loop cannot be found fragment databases may be searched for loops in other proteins that may provide a suitable model for the unknown. If desired, the loop may then be subjected to conformational searching to identify low energy conformers if desired.

[0240] Once a homology model has been generated it is analyzed to determine its correctness. A computer program available to assist in this analysis is the Protein Health module in Quanta which provides a variety of tests. Other programs that provide structure analysis along with output include PROCHECK and 3D-Profiler [Luthy R. et al, Nature 356: 83-85, 1992; and Bowie, J. U. et al, Science 253: 164-170, 1991]. Once any irregularities have been resolved, the entire structure may be further refined. Refinement may consist of energy minimization with restraints, especially for the SCRs. Restraints may be gradually removed for subsequent minimizations. Molecular dynamics may also be applied in conjunction with energy minimization.

[0241] Molecular replacement involves applying a known structure to solve the X-ray crystallographic data set of a polypeptide of unknown structure. The method can be used to define the phases describing the X-ray diffraction data of a polypeptide of unknown structure when only the amplitudes are known. Thus in an embodiment of the invention, a method is provided for determining three dimensional structures of polypeptides with unknown structure by applying the structural coordinates of the crystal of the present invention to provide an X-ray crystallographic data set for a polypeptide of unknown structure, and (b) determining a low energy conformation of the resulting structure.

[0242] The structural coordinates of the crystal of the present invention may be applied to nuclear magnetic resonance (NMR) data to determine the three dimensional structures of polypeptides with uncharacterised or incompletely characterised structure. (See for example, Wuthrich, 1986, John Wiley and Sons, New York: 176-199; Pflugrath et al., 1986, J. Molecular Biology 189: 383-386; Kline et al., 1986 J. Molecular Biology 189:377-382). While the secondary structure of a polypeptide may often be determined by NMR data, the spatial connections between individual pieces of secondary structure are not as readily determined. The structural co-ordinates of a polypeptide defined by X-ray crystallography can guide the NMR spectroscopist to an understanding of the spatial interactions between secondary structural elements in a polypeptide of related structure. Information on spatial interactions between secondary structural elements can greatly simplify Nuclear Overhauser Effect (NOE) data from two-dimensional NMR experiments. In addition, applying the structural co-ordinates after the determination of secondary structure by NMR techniques simplifies the assignment of NOE's relating to particular amino acids in the polypeptide sequence and does not greatly bias the NMR analysis of polypeptide structure.

[0243] In an embodiment, the invention relates to a method of determining three dimensional structures of polypeptides with unknown structures, by applying the structural coordinates of a crystal of the present invention to nuclear magnetic resonance (NMR) data of the unknown structure. This method comprises the steps of: (a) determining the secondary structure of an unknown structure using NMR data; and (b) simplifying the assignment of through-space interactions of amino acids. The term “through-space interactions” defines the orientation of the secondary structural elements in the three dimensional structure and the distances between amino acids from different portions of the amino acid sequence. The term “assignment” defines a method of analyzing NMR data and identifying which amino acids give rise to signals in the NMR spectrum.

[0244] Screening Method

[0245] The present invention also provides a method of screening for a ligand that associates with a ligand binding pocket and/or modulates the function of a glycosyltransferase, by using a crystal or a model according to the present invention. The method may involve investigating whether a test compound is capable of associating with or binding a ligand binding pocket.

[0246] As used herein, the term “test compound” refers to any compound which is potentially capable of associating with a ligand binding pocket and/or modulating the function of a glycosyltransferase. If, after testing, it is determined that a test compound does bind to a LBP, it is known as a “ligand”.

[0247] A “test compound” includes but is not limited to, a compound which may be obtainable from or produced by any suitable source, whether natural or not. The test compound may be designed or obtained from a library of compounds which may comprise peptides, as well as other compounds, such as small organic molecules and particularly new lead compounds. By way of example, the test compound may be a natural substance, a biological macromolecule, or an extract made from biological materials such as bacteria, fungi, or animal (particularly mammalian) cells or tissues, an organic or an inorganic molecule, a synthetic test compound, a semi-synthetic test compound, a carbohydrate, a monosaccharide, an oligosaccharide or polysaccharide, a glycolipid, a glycopeptide, a saponin, a heterocyclic compound, a structural or functional mimetic, a peptide, a peptidomimetic, a derivatised test compound, a peptide cleaved from a whole protein, or a peptides synthesised synthetically (such as, by way of example, either using a peptide synthesizer or by recombinant techniques or combinations thereof), a recombinant test compound, a natural or a non-natural test compound, a fusion protein or equivalent thereof and mutants, derivatives or combinations thereof.

[0248] The test compound may be screened as part of a library or a data base of molecules. Data bases which may be used include ACD (Molecular Designs Limited), NCI (National Cancer Institute), CCDC (Cambridge Crystallographic Data Center), CAST (Chemical Abstract Service), Derwent (Derwent Information Limited), Maybridge (Maybridge Chemical Company Ltd), Aldrich (Aldrich Chemical Company), DOCK (University of California in San Francisco), and the Directory of Natural Products (Chapman & Hall). Computer programs such as CONCORD (Tripos Associates) or DB-Converter (Molecular Simulations Limited) can be used to convert a data set represented in two dimensions to one represented in three dimensions.

[0249] Test compounds may be tested for their capacity to fit spatially into the glycosyltransferase LBP. As used herein, the term “fits spatially” means that the three-dimensional structure of the test compound is accommodated geometrically in a cavity or pocket of the glycosyltransferase LBP. The test compound can then be considered to be a ligand.

[0250] A favourable geometric fit occurs when the surface areas of the test compound are in close proximity with the surface area of the cavity or pocket without forming unfavorable interactions. A favourable complementary interaction occurs where the test compound interacts by hydrophobic, aromatic, ionic, dipolar, or hydrogen donating and accepting forces. Unfavourable interactions may be steric hindrance between atoms in the test compound and atoms in the binding site.

[0251] In an embodiment of the invention, a method is provided for identifying potential modulators of a glycosyltransferase function. The method utilizes the structural coordinates or model of a glycosyltransferase three dimensional structure, or binding pocket thereof. The method comprises the steps of (a) docking a computer representation of a test compound from a computer data base with a computer model of a ligand binding pocket of a glycosyltransferase; (b) determining a conformation of a complex between the test compound and binding pocket with a favourable geometric fit or favorable complementary interactions; and (c) identifying test compounds that best fit the glycosyltransferase ligand binding pocket as potential modulators of glycosyltransferase function. The initial glycosyltransferase structure may or may not have ligands including substrates bound to it. A favourable complementary interaction occurs where a compound in a compound-glycosyltransferase complex interacts by hydrophobic, ionic, or hydrogen donating and accepting forces, with the active-site or binding pocket of a glycosyltransferase without forming unfavorable interactions.

[0252] If a model of the present invention is a computer model, the test compounds may be positioned in an LBP through computational docking. If, on the other hand, the model of the present invention is a structural model, the test compounds may be positioned in the LBP by, for example, manual docking.

[0253] As used herein the term “docking” refers to a process of placing a compound in close proximity with a glycosyltransferase LBP, or a process of finding low energy conformations of a test compound/glycosyltransferase complex.

[0254] A screening method of the present invention may comprise the following steps:

[0255] (i) generating a computer model of a glycosyltransferase or a ligand binding pocket thereof using a crystal according to the invention;

[0256] (ii) docking a computer representation of a test compound with the computer model;

[0257] (iii) analysing the fit of the compound in the glycosyltransferase or ligand binding pocket.

[0258] The method may be applied to a plurality of test compounds, to identify those that best fit the enzyme or ligand binding pocket.

[0259] In an aspect of the invention a method is provided comprising the following steps:

[0260] (a) docking a computer representation of a structure of a test compound into a computer representation of a ligand binding pocket of a glycosyltransferase defined in accordance with the invention using a computer program, or by interactively moving the representation of the test compound into the representation of the binding pocket;

[0261] (b) characterizing the geometry and the complementary interactions formed between the atoms of the ligand binding pocket and the compound; optionally

[0262] (c) searching libraries for molecular fragments which can fit into the empty space between the compound and ligand binding pocket and can be linked to the compound; and

[0263] (d) linking the fragments found in (c) to the compound and evaluating the new modified compound.

[0264] In an embodiment of the invention a method is provided which comprises the following steps:

[0265] (a) docking a computer representation of a test compound from a computer data base with a computer representation of a selected site (e.g. an inhibitor binding pocket) on a glycosyltransferase structure or model defined in accordance with the invention to obtain a complex;

[0266] (b) determining a conformation of the complex with a favourable geometric fit and favourable complementary interactions; and

[0267] (c) identifying test compounds that best fit the selected site as potential modulators of the glycosyltransferase.

[0268] The model used in the screening method may comprise the ligand-binding pocket of a glycosyltransferase enzyme either alone or in association with one or more ligands and/or cofactors. For example, the model may comprise the ligand-binding pocket in association with a donor molecule (or analogue thereof) and/or an acceptor molecule (or analogue thereof).

[0269] If the model comprises an unassociated ligand binding pocket, then the selected site under investigation may be the LBP itself. The test compound may, for example, mimic a known substrate for the enzyme (such as a donor or acceptor molecule) in order to interact with the LBP. The selected site may alternatively be another site on the enzyme (for example a site involved in attachment to the bacterial membrane).

[0270] If the model comprises an associated LBP, for example an LBP in association with a donor molecule or analogue thereof, the selected site may be the LBP or a site made up of the LBP and the complexed ligand, or a site on the ligand itself. The test compound may be investigated for its capacity to modulate the interaction with the associated molecule.

[0271] A test compound (or plurality of test compounds) may be selected on the basis of its similarity to a known ligand for the glycosyltransferase. For example, the screening method may comprise the following steps:

[0272] (i) generating a computer model of the LBP of a glycosyltransferase in complex with a ligand;

[0273] (ii) searching for a test compound with a similar three dimensional structure and/or similar chemical groups; and

[0274] (iii) evaluating the fit of the test compound in the LBP.

[0275] Searching may be carried out using a database of computer representations of potential compounds, using methods known in the art.

[0276] The present invention also provides a method for designing ligands for a glycosyltransferase. It is well known in the art to use a screening method as described above to identify a test compound with promising fit, but then to use this test compound as a starting point to design a ligand with improved fit to the model. Such techniques are known as “structure-based ligand design” (See Kuntz et al., 1994, Ace. Chem. Res. 27:117; Guida, 1994, Current Opinion in Struc. Biol. 4: 777; and Colman, 1994, Current Opinion in Struc. Biol. 4: 868, for reviews of structure-based drug design and identification;and Kuntz et al 1982, J. Mol. Biol. 162:269; Kuntz et al., 1994, Acc. Chem. Res. 27: 117; Meng et al., 1992, J. Compt. Chem. 13: 505; Bohm, 1994, J. Comp. Aided Molec. Design 8: 623 for methods of structure-based modulator design).

[0277] Examples of computer programs that may be used for structure-based ligand design are CAVEAT (Bartlett et al., 1989, in “Chemical and Biological Problems in Molecular Recognition”, Roberts, S. M. Ley, S. V.; Campbell, N. M. eds; Royal Society of Chemistry: Cambridge, pp 182-196); FLOG Miller et al., 1994, J. Comp. Aided Molec. Design 8:153); PRO Modulator (Clark et al., 1995 J. Comp. Aided Molec. Design 9:13); MCSS (Miranker and Karplus, 1991, Proteins: Structure, Function, and Genetics 8:195); and, GRID (Goodford, 1985, J. Med. Chem. 28:849).

[0278] The method may comprise the following steps:

[0279] (i) docking a model of a test compound with a model of a selected site;

[0280] (ii) identifying one or more groups on the test compound which may be modified to improve their fit in the selected site;

[0281] (iii) replacing one or more identified groups to produce a modified test compound model; and

[0282] (iv) docking the modified test compound model with the model of the selected site.

[0283] Evaluation of fit may comprise the following steps:

[0284] (a) mapping chemical features of a test compound such as by hydrogen bond donors or acceptors, hydrophobic/lipophilic sites, positively ionizable sites, or negatively ionizable sites; and

[0285] (b) adding geometric constraints to selected mapped features.

[0286] The fit of the modified test compound may then be evaluated using the same criteria.

[0287] The chemical modification of a group may either enhance or reduce hydrogen bonding interaction, charge interaction, hydrophobic interaction, Van Der Waals interaction or dipole interaction between the test compound and the key amino acid residue(s) of the selected site. Preferably the group modifications involve the addition, removal, or replacement of substituents onto the test compound such that the substituents are positioned to collide or to bind preferentially with one or more amino acid residues that correspond to the key amino acid residues of the selected site.

[0288] Identified groups in a test compound may be substituted with, for example, alkyl, alkoxy, hydroxyl, aryl, cycloalkyl, alkenyl, alkynyl, thiol, thioalkyl, thioaryl, amino, or halo groups. Generally, initial substitutions are conservative, i.e., the replacement group will have approximately the same size, shape, hydrophobicity and charge as the original group. It should, of course, be understood that components known in the art to alter conformation should be avoided.

[0289] If a modified test compound model has an improved fit, then it may bind to the selected site and be considered to be a “ligand”. Rational modification of groups may be made with the aid of libraries of molecular fragments which may be screened for their capacity to fit into the available space and to interact with the appropriate atoms. Databases of computer representations of libraries of chemical groups are available commercially, for this purpose.

[0290] The test compound may also be modified “in situ” (i.e. once docked into the potential binding site), enabling immediate evaluation of the effect of replacing selected groups. The computer representation of the test compound may be modified by deleting a chemical group or groups, or by adding a chemical group or groups. After each modification to a compound, the atoms of the modified compound and potential binding site can be shifted in conformation and the distance between the compound and the active site atoms may be scored on the basis of geometric fit and favourable complementary interactions between the molecules. This technique is described in detail in Molecular Simulations User Manual, 1995 in LUDI.

[0291] Examples of ligand building and/or searching computer include programs in the Molecular Simulations Package (Catalyst), ISIS/HOST, ISIS/BASE, and ISIS/DRAW (Molecular Designs Limited), and UNITY (Tripos Associates).

[0292] The “starting point” for rational ligand design may be a known ligand for the enzyme. For example, in order to identify potential modulators of the glycosyltransferase, a logical approach would be to start with a known ligand (for example a donor or acceptor molecule) to produce a molecule which mimics the binding of the ligand. Such a molecule may, for example, act as a competitive inhibitor for the true ligand, or may bind so strongly that the interaction (and inhibition) is effectively irreversible.

[0293] Such a method may comprise the following steps:

[0294] (i) generating a computer model of a LBP of a glycosyltransferase in complex with a ligand;

[0295] (ii) replacing one or more groups on the ligand model to produce a modified ligand; and

[0296] (iii) evaluating the fit of the modified ligand in the LBP.

[0297] The replacement groups could be selected and replaced using a compound construction program which replaces computer representations of chemical groups with groups from a computer database, where the representations of the compounds are defined by structural co-ordinates.

[0298] In an embodiment, a screening method is provided for identifying a ligand of a glycosyltransferase comprising the step of using the structural co-ordinates of a donor molecule or acceptor molecule or component thereof, defined in relation to its spatial association with a glycosyltransferase structure or a ligand binding pocket of the invention, to generate a compound that is capable of associating with the glycosyltransferase or ligand binding pocket.

[0299] The screening methods of the present invention may be used to identify compounds or entities that associate with a molecule that associates with a glycosyltransferase enzyme (for example, a substrate molecule).

[0300] In an embodiment of the invention, a screening method is provided for identifying a ligand of a glycosyltransferase comprising the step of using the structural co-ordinates of uridine, uracil, or UDP listed in Table 4, 5, or 6 to generate a compound for associating with the active site binding pocket of a glycosyltransferase as described herein. The following steps are employed in a particular method of the invention: (a) generating a computer representation of uridine, uracil, or UDP, defined by its structural coordinates listed in Table 4, 5, or 6; (b) searching for molecules in a data base that are structurally or chemically similar to the defined uridine, uracil, or UDP, using a searching computer program, or replacing portions of the compound with similar chemical structures from a database using a compound building computer program.

[0301] In another embodiment of the invention, a screening method is provided for identifying a ligand of a glycosyltransferase comprising the step of using the structural co-ordinates of UDP-Gal listed in Table 4, 5, or 6 to generate a compound for associating with the active site of a glycosyltransferase of the invention. The following steps are employed in a particular method of the invention: (a) generating a computer representation of UDP-Gal defined by its structural co-ordinates listed in Table 4, 5, or 6; and (b) searching for molecules in a data base that are structurally or chemically similar to the defined UDP-Gal using a searching computer program, or replacing portions of the compound with similar chemical structures from a database using a compound building computer program.

[0302] In another embodiment of the invention, a method is provided for designing potential inhibitors of a glycosyltransferase comprising the step of using the structural coordinates of a lactose molecule in Table 5, to generate a compound for associating with the active site of a glycosyltransferase.

[0303] The following steps are employed in a particular method of the invention: (a) generating a computer representation of a lactose acceptor defined by its structural coordinates listed in Table 4, 5, or 6; and (b) searching for molecules in a data base that are structurally or chemically similar to the defined lactose acceptor using a searching computer program, or replacing portions of the compound with similar chemical structures from a database using a compound building computer program.

[0304] The screening methods of the present invention may be used to identify compounds or entities that associate with a molecule that associates with a glycosyltransferase enzyme (for example, a donor or acceptor molecule).

[0305] Compounds and entities (e.g. ligands) of glycosyltransferases identified using the above-described methods may be prepared using methods described in standard reference sources utilized by those skilled in the art. For example, organic compounds may be prepared by organic synthetic methods described in references such as March, 1994, Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, New York, McGraw Hill.

[0306] Test compounds and ligands which are identified using a model of the present invention can be screened in assays such as those well known in the art. Screening can be, for example, in vitro, in cell culture, and/or in vivo. Biological screening assays preferably centre on activity-based response models, binding assays (which measure how well a compound binds), and bacterial, yeast and animal cell lines (which measure the biological effect of a compound in a cell). The assays can be automated for high capacity-high throughput screening (HTS) in which large numbers of compounds can be tested to identify compounds with the desired activity. The biological assay, may also be an assay for the ligand binding activity of a compound that selectively binds to the ligand binding domain compared to other enzymes.

[0307] Ligands/Compounds/Modulators

[0308] The present invention provides a ligand or compound or entity identified by a screening method of the present invention. A ligand or compound may have been designed rationally by using a model according to the present invention. A ligand or compound identified using the screening methods of the invention specifically associate with a target compound. In the present invention the target compound may be the glycosyltransferase enzyme or a molecule that is capable of associating with the glycosyltransferase enzyme (for example a donor or acceptor molecule). In a preferred embodiment the ligand is capable of binding to the LBP of a glycosyltransferase.

[0309] A ligand or compound identified using a screening method of the invention may act as a “modulator”, i.e. a compound which affects the activity of a glycosyltransferase. A modulator may reduce, enhance or alter the biological function of a glycosyltransferase. For example a modulator may modulate the capacity of the enzyme to transfer a sugar from donor to acceptor. Alternatively, or in addition, it may modulate the capacity of the enzyme to attach to bacterial membranes. An alteration in biological function may be characterised by a change in specificity. For example, a modulator may cause the enzyme to accept a different acceptor or donor molecule, to transfer a different sugar, or to work with a different metal cofactor. In order to exert its function, the modulator commonly binds to the ligand binding pocket.

[0310] A “modulator” which is capable of reducing the biological function of the enzyme may also be known as an inhibitor. Preferably an inhibitor reduces or blocks the capacity of the enzyme to transfer a sugar from donor to acceptor. The inhibitor may mimic the binding of a donor or acceptor molecule, for example, it may be a donor or acceptor analogue. A donor or acceptor analogue may be designed by considering the interactions between the donor or acceptor molecule and the enzyme (for example by using information derivable from the crystal of the invention) and specifically altering one or more groups (as described above). Examples of donor and acceptor molecule analogues for LgtC are UDP-2Fgal and 4-deoxylactose respectively. Acceptor molecule analogues are also illustrated in Example 2.

[0311] In a highly preferred embodiment a modulator acts as an inhibitor of the glycosyltransferase and is capable of inhibiting lipooligosaccharide biosynthesis. Such an inhibitor may be useful as an antibiotic, because inhibition of LOS synthesis will prevent the bacterium from escaping detection by the human immune system by minicing human glycoproteins.

[0312] The present invention also provides a method for modulating the activity of a glycosyltransferase within a bacterial cell using a modulator according to the present invention. It would be possible to monitor the expression of LOS on the bacterial surface following such treatment by a number of methods known in the art (for example by detecting expression with an LOS-specific antibody).

[0313] In another preferred embodiment, the modulator is capable of causing or preventing oxidation of Cys 246. It is thought that oxidation of Cys 246 results in impaired donor and acceptor binding.

[0314] In another preferred embodiment, the modulator modulates the catalytic mechanism of the enzyme. For example it may affect the capacity of the side-chain oxygen of Gln 189 to act as a nucleophile in the double displacement mechanism.

[0315] A modulator may be an agonist, partial agonist, partial inverse agonist or antagonist of the glucosyltransferase.

[0316] As used herein, the term “agonist” means any ligand, which is capable of binding to a ligand binding pocket and which is capable of increasing a proportion of the enzyme that is in an active form, resulting in an increased biological response. The term includes partial agonists and inverse agonists.

[0317] As used herein, the term “partial agonist” means an agonist that is unable to evoke the maximal response of a biological system, even at a concentration sufficient to saturate the specific receptors.

[0318] As used herein, the term “partial inverse agonist” is an inverse agonist that evokes a submaximal response to a biological system, even at a concentration sufficient to saturate the specific receptors. At high concentrations, it will diminish the actions of a full inverse agonist.

[0319] The invention relates to a glycosyltransferase ligand binding pocket antagonist, wherein said ligand binding pocket is that defined by the amino acid structural coordinates described herein. For example the ligand may antagonise the inhibition of glycosyltransferase by an inhibitor.

[0320] As used herein, the term “antagonist” means any agent that reduces the action of another agent, such as an agonist. The antagonist may act at the same site as the agonist (competitive antagonism). The antagonistic action may result from a combination of the substance being antagonised (chemical antagonism) or the production of an opposite effect through a different receptor (functional antagonism or physiological antagonism) or as a consequence of competition for the binding site of an intermediate that links receptor activation to the effect observed (indirect antagonism).

[0321] As used herein, the term “competitive antagonism” refers to the competition between an agonist and an antagonist for a receptor that occurs when the binding of agonist and antagonist becomes mutually exclusive. This may be because the agonist and antagonist compete for the same binding site or combine with adjacent but overlapping sites. A third possibility is that different sites are involved but that they influence the receptor macromolecules in such a way that agonist and antagonist molecules cannot be bound at the same time. If the agonist and antagonist form only short lived combinations with the receptor so that equilibrium between agonist, antagonist and receptor is reached during the presence of the agonist, the antagonism will be surmountable over a wide range of concentrations. In contrast, some antagonists, when in close enough proximity to their binding site, may form a stable covalent bond with it and the antagonism becomes insurmountable when no spare receptors remain.

[0322] As mentioned above, an identified ligand or compound may act as a ligand model (for example, a template) for the development of other compounds. A modulator may be a mimetic of a ligand or ligand binding pocket A mimetic of a ligand (e.g an acceptor or donor molecule or part thereof) may compete with a natural ligand for a glycosyltransferase and antagonize a physiological effect of the enzyme in an animal. A mimetic of a ligand may be an organically synthesized compound. A mimetic of a ligand binding pocket, may be either a peptide or other biopharmaceutical (such as an organically synthesized compound) that specifically binds to a natural acceptor or donor molecule for a glycosyltransferase and antagonizes a physiological effect of the enzyme in an animal.

[0323] Once a ligand has been optimally selected or designed, substitutions may then be made in some of its atoms or side groups in order to improve or modify its binding properties. Generally, initial substitutions are conservative, i.e., the replacement group will have approximately the same size, shape, hydrophobicity and charge as the original group. It should, of course, be understood that components known in the art to alter conformation should be avoided. Such substituted chemical compounds may then be analyzed for efficiency of fit to a glycosyltransferase ligand binding pocket by the same computer methods described above. Preferably, positions for substitution are selected based on the predicted binding orientation of a ligand to a glycosyltransferase ligand binding pocket.

[0324] A modulator may be one or a variety of different sorts of molecule. For example, a modulator may be a peptide, member of random peptide libraries and combinatorial chemistry-derived molecular libraries, phosphopeptide (including members of random or partially degenerate, directed phosphopeptide libraries), a carbohydrate, a monosaccharide, an oligosaccharide or polysaccharide, a glycolipid, a glycopeptide, a saponin, a heterocyclic compound antibody, carbohydrate, nucleoside or nucleotide or part thereof, and small organic or inorganic molecule. A modulator may be an endogenous physiological compound, or it may be a natural or synthetic compound. The modulators of the present invention may be natural or synthetic. The term “modulator” also refers to a chemically modified ligand or compound.

[0325] A technique suitable for preparing a modulator will depend on its chemical nature. For example, peptides can be synthesized by solid phase techniques (Roberge J Y et al (1995) Science 269: 202-204) and automated synthesis may be achieved, for example, using the ABI 43 1 A Peptide Synthesizer (Perlin Elmer) in accordance with the instructions provided by the manufacturer. Once cleaved from the resin, the peptide may be purified by preparative high performance liquid chromatography (e.g., Creighton (1983) Proteins Structures and Molecular Principles, W H Freeman and Co, New York N.Y.). The composition of the synthetic peptides may be confirmed by amino acid analysis or sequencing (e.g., the Edman degradation procedure; Creighton, supra).

[0326] If a modulator is a nucleotide, or a polypeptide expressable therefrom, it may be synthesized, in whole or in part, using chemical methods well known in the art (see Caruthers M H et al (1980) Nuc Acids Res Symp Ser 215-23, Horn T et al (1980) Nuc Acids Res Symp Ser 225-232), or it may be prepared using recombinant techniques well known in the art.

[0327] Organic compounds may be prepared by organic synthetic methods described in references (e.g. March, 1994, Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, New York, McGraw Hill).

[0328] The invention also relates to classes of modulators of glycosyltransferases based on the structure and shape of a ligand, in particular, a substrate including a donor molecule, or component thereof, or an acceptor molecule or component thereof, defined in relation to the ligand's spatial association with a glycosyltransferase structure of the invention or part thereof. Therefore, a modulator may comprise a ligand, in particular a donor molecule or an acceptor molecule, having the shape or structure, preferably the structural coordinates, of the ligand in the active site binding pocket of a reaction catalyzed by a glycosyltransferase.

[0329] A class of modulators of glycosyltransferases may comprise a compound containing a structure of uracil, uridine, ribose, pyrophosphate, or UDP, and having one or more, preferably all, of the structural coordinates of uracil, uridine, ribose, pyrophosphate, or UDP of Table 4, 5, or 6. In an embodiment, modulators are provided comprising the structure of UDP-Gal and having one or more, preferably all, of the structural co-ordinates of UDP-Gal of Table 4, 5, or 6. Functional groups in the uracil, uridine, ribose, pyrophosphate, UDP, or UDP-Gal modulators may be substituted with, for example, alkyl, alkoxy, hydroxyl, aryl, cycloalkyl, alkenyl, allynyl, thiol, thioalkyl, thioaryl, amino, or halo, or they may be modified using techniques known in the art. Substituents will be selected to optimize the activity of the modulator.

[0330] Modulators are also contemplated that comprise the structure of an acceptor molecule with the structural co-ordinates of lactose in Table 5 or 6. Functional groups in an acceptor structure may be substituted with, for example, alkyl, alkoxy, hydroxyl, aryl, cycloalkyl, alkenyl, alkynyl, thiol, thioalkyl, thioaryl, amino, or halo, or they may be modified using techniques known in the art. Substituents will b selected to optimize the activity of the modulator.

[0331] A class of modulators defined by the invention are compounds comprising the structural coordinates of UDP-Gal in the active site binding pocket of a reaction catalyzed by a glycosyltransferase. The UDP-Gal adopts a folded conformation in which the UDP moiety is bound in an extended manner and the galactose tucks back under the phosphates such that the plane of the galactose ring is almost parallel to the plane of the diphosphate (FIGS. 3).

[0332] Another class of modulators of the invention are compounds comprising a uridine diphosphate group having the structural co-ordinates of uridine diphosphate in the active site binding pocket of a reaction catalyzed by a glycosyltransferase.

[0333] Yet another class of modulators defined by the invention are compounds comprising the structural co-ordinates of lactose or an analogue thereof (4-deoxylactose, see also Example 2) in the active site binding pocket of a reaction catalyzed by a glycosyltransferase. The moieties of the lactose adopt a full chair conformation.

[0334] A class of modulators contemplated by the present invention are donor-acceptor complexes based on the spatial arrangement of a donor molecule and acceptor molecule in a transition state in a glycosyltransferase reaction. While not wishing to be bound by any particular theory, a retaining glycosyltransferase of the present invention may follow an SNi mechanism involving a direct displacement of the leaving group by the nucleophile, but from the front face of the sugar. Thus both the 4-hydroxyl of the lactose acceptor (the nucleophile) and the phosphate moiety of the UDP leaving group are located on the alpha face of the sugar. Reaction proceeds via a very dissociative (oxocarbenium ion-like) transition state. Precedent exists for this type of mechanism. (See J. Org Chem. (1994) 59, 1849; J. Org Chem. (1989) 54, 761;J. Org Chem. (1993), 58, 2822; see J. Amer Chem Soc (1980) 102, 2026:J. Amer. Chem. Soc. (1990) 10 113, 7958 re sugar systems). Based on this mechanism, the invention contemplates the following classes of modulators:

[0335] The invention contemplates all optical isomers and racemic forms of the modulators of the invention.

[0336] Pharmaceutical Composition

[0337] The present invention also provides the use of a ligand, in particular a modulator according to the invention, in the manufacture of a medicament to treat and/or prevent a disease in a mammalian patient. There is also provided a pharmaceutical composition comprising such a ligand or modulator and a method of treating and/or preventing a disease comprising the step of administering such a ligand or modulator or pharmaceutical composition to a mammalian patient.

[0338] The pharmaceutical compositions may be for human or animal usage in human and veterinary medicine and will typically comprise a pharmaceutically acceptable carrier, diluent, excipient, adjuvant or combination thereof.

[0339] Acceptable carriers or diluents for therapeutic use are well known in the pharmaceutical art, and are described, for example, in Remington's Pharmaceutical Sciences, Mack Publishing Co. (A. R. Gennaro edit. 1985). The choice of pharmaceutical carrier, excipient or diluent can be selected with regard to the intended route of administration and standard pharmaceutical practice. The pharmaceutical compositions may comprise in addition to the carrier, excipient or diluent any suitable binder(s), lubricant(s), suspending agent(s), coating agent(s), and solubilising agent(s).

[0340] Preservatives, stabilizers, dyes and even flavouring agents may be provided in the pharmaceutical composition. Examples of preservatives include sodium benzoate, sorbic acid and esters of p-hydroxybenzoic acid Antioxidants and suspending agents may be also used.

[0341] The routes for admininstration (delivery) include, but are not limited to, one or more of: oral (e.g. as a tablet, capsule, or as an ingestable solution), topical, mucosal (e.g. as a nasal spray or aerosol for inhalation), nasal, parenteral (e.g. by an injectable form), gastrointestinal, intraspinal, intraperitoneal, intramuscular, intravenous, intrauterine, intraocular, intradermal, intracranial, intratracheal, intravaginal, intracerebroventricular, intracerebral, subcutaneous, ophthalmic (including intravitreal or intracameral), transdermal, rectal, buccal, vaginal, epidural, sublingual.

[0342] Where the pharmaceutical composition is to be delivered mucosally through the gastrointestinal mucosa, it should be able to remain stable during transit though the gastrointestinal tract; for example, it should be resistant to proteolytic degradation, stable at acid pH and resistant to the detergent effects of bile.

[0343] Where appropriate, the pharmaceutical compositions can be administered by inhalation, in the form of a suppository or pessary, topically in the form of a lotion, gel, hydrogel, solution, cream, ointment or dusting powder, by use of a skin patch, orally in the form of tablets containing excipients such as starch or lactose or chalk, or in capsules or ovules either alone or in admixture with excipients, or in the form of elixirs, solutions or suspensions containing flavouring or colouring agents, or they can be injected parenterally, for example intravenously, intramuscularly or subcutaneously. For parenteral administration, the compositions may be best used in the form of a sterile aqueous solution which may contain other substances, for example enough salts or monosaccharides to make the solution isotonic with blood. The aqueous solutions should be suitably buffered (preferably to a pH of from 3 to 9), if necessary. The preparation of suitable parenteral formulations under sterile conditions is readily accomplished by standard pharmaceutical techniques well-known to those skilled in the art.

[0344] If the agent of the present invention is administered parenterally, then examples of such administration include one or more of: intravenously, intra-arterially, intraperitoneally, intrathecally, intraventricularly, intraurethrally, intrasternally, intracranially, intramuscularly or subcutaneously administering the agent; and/or by using infusion techniques.

[0345] For buccal or sublingual administration the compositions may be administered in the form of tablets or lozenges which can be formulated in a conventional manner.

[0346] The tablets may contain excipients such as microcrystalline cellulose, lactose, sodium citrate, calcium carbonate, dibasic calcium phosphate and glycine, disintegrants such as starch (preferably corn, potato or tapioca starch), sodium starch glycollate, croscarmellose sodium and certain complex silicates, and granulation binders such as polyvinylpyrrolidone, hydroxypropylmethylcellulose (HPMC), hydroxypropylcellulose (HPC), sucrose, gelatin and acacia. Additionally, lubricating agents such as magnesium stearate, stearic acid, glyceryl behenate, and talc may be included.

[0347] Solid compositions of a similar type may also be employed as fillers in gelatin capsules. Preferred excipients in this regard include lactose, starch, cellulose, milk sugar, or high molecular weight polyethylene glycols. For aqueous suspensions and/or elixirs, the agent may be combined with various sweetening or flavouring agents, colouring matter or dyes, with emulsifying and/or suspending agents, and with diluents such as water, ethanol, propylene glycol and glycerin, and combinations thereof.

[0348] As indicated, a therapeutic agent of the present invention can be administered intranasally or by inhalation and is conveniently delivered in the form of a dry powder inhaler or an aerosol spray presentation from a pressurised container, pump, spray or nebuliser with the use of a suitable propellant, e.g. dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, a hydrofluoroalkane such as 1,1,1,2-tetrafluoroethane (HFA 134A™m) or 1,1,1,2,3,3,3-heptafluoropropane (HFA 227EA™), carbon dioxide or other suitable gas. In the case of a pressurised aerosol, the dosage unit may be determined by providing a valve to deliver a metered amount The pressurised container, pump, spray or nebuliser may contain a solution or suspension of the active compound, e.g. using a mixture of ethanol and the propellant as the solvent, which may additionally contain a lubricant, e.g. sorbitan trioleate. Capsules and cartridges (made, for example, from gelatin) for use in an inhaler or insufflator may be formulated to contain a powder mix of the agent and a suitable powder base such as lactose or starch.

[0349] Therapeutic administration of polypeptide ligands (e.g. modulators) may also be accomplished using gene therapy. A nucleic acid including a promoter operatively linked to a heterologous polypeptide may be used to produce high-level expression of the polypeptide in cells transfected with the nucleic acid. DNA or isolated nucleic acids may be introduced into cells of a subject by conventional nucleic acid delivery systems. Suitable delivery systems include liposomes, naked DNA, and receptor-mediated delivery systems, and viral vectors such as retroviruses, herpes viruses, and adenoviruses.

[0350] The invention further provides a method of treating a mammal, the method comprising administering to a mammal a ligand (e.g. modulator) or pharmaceutical composition of the present invention.

[0351] Typically, a physician will determine the actual dosage which will be most suitable for an individual subject and it will vary with the age, weight and response of the particular patient and severity of the condition. The dosages below are exemplary of the average case. There can, of course, be individual instances where higher or lower dosage ranges are merited.

[0352] The specific dose level and frequency of dosage for any particular patient may be varied and will depend upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of that compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the individual undergoing therapy. By way of example, the pharmaceutical composition of the present invention may be administered in accordance with a regimen of 1 to 10 times per day, such as once or twice per day.

[0353] For oral and parenteral administration to human patients, the daily dosage level of the agent may be in single or divided doses.

[0354] Applications

[0355] As mentioned above, some glycosyltransferases are involved in the biosynthesis of bacterial lipooligosaccharide (LOS) which is thought to be essential for the pathogen to attach to host receptors and to evade the immune response (Kahler C M, Stephens D S, Crit Rev Microbiol 1998;24(4):281-334). A ligand or modulator may be able to modulate the activity of a glycosyltransferase within a bacterial cell. Hence a ligand or modulator according to the present invention may be capable of modulating LOS synthesis and therefore modulating bacterial attachment and/or recognition by the immune system.

[0356] Lipooligosaccharides (LOSs) are expressed on mucosal Gram-negative bacteria, including members of the genera Neisseria, Haemophilus, Bordetella, and Branhamella. They can also be expressed on some enteric bacteria such as Campylobacter jejuni and Campylobacter coli strains. LOSs share similar lipid A structures with an identical array of functional activities as LPSs. LOSs lack O-antigen units with the LOS oligosaccharide structures limited to 10 saccharide units. The LOS species of pathogenic Neisseria can play a major role in pathogenesis through enhancing the resistance of the organism to killing by normal human serum. Other distinguishing characteristics of LOS are the structural and antigenic similarity of some LOS species to human glycolipids and the potential for certain LOSs to be modified in vivo by host substances or secretions. These modifications of LOS in different environments of the host result in synthesis of new LOS structures that probably benefit the survival of the pathogen. The LOS of N. gonorrhoeae can act as a ligand of human receptors, promoting invasion of host cells.

[0357] Therefore, a ligand or modulator of the invention may be used to treat diseases caused by the following pathogenic organisms that have a LOS/LPS involvement in disease: Neisseria (meningitidis and gonnhorea) Haemophilus (influenzae and ducreyii), Branhanella (Moraxella), Canplyobacter, and Helicobacter. In a preferred embodiment the disease is associated with infection by a bacterium from the species Neisseria In a highly preferred embodiment the disease is associated with infection by Neisseria meningitidis, such diseases include, but are not limited to meningitis.

[0358] Meningococcal LOS is a critical virulence factor in N. meningitidis infections and is involved in many aspects of pathogenesis, including the colonization of the human nasopharynx, survival after bloodstream invasion, and the inflammation associated with the morbidity and mortality of meningococcemia and meningitis. Meningococcal LOS, which is a component of serogroup B meningococcal vaccines currently in clinical trials, has been proposed as a candidate for a new generation of meningococcal vaccines. (FEMS Immunol Med Microbiol 1996 Dec 1;16(2):105-15 Moran A P, Prendergast M M, Appelmelk B J)

[0359] LOS of pathogenic Neisseria spp. mimic the carbohydrate moieties of glycosphingolipids present on human cells. Such mimicry may serve to camouflage the bacterial surface from the host The LOS component is antigenically and/or chemically identical to lactoneoseries glycosphingolipids and can become sialylated in Neisseria gonorrhoeae when the bacterium is grown in the presence of cytidine 5′-monophospho-N-acetylneuraminic acid, the nucleotide sugar of sialic acid Strains of Neisseria meningitidis and Haemophilus influenzae also express similarly sialylated LPS. Sialylation of the LOS influences susceptibility to bactericidal antibody, may decrease or prevent phagocytosis, cause down-regulation of complement activation, and decrease adherence to neutrophils and the subsequent oxidative burst response. The core oligosaccharides of LPS of Campylobacter jejuni serotypes which are associated with the development of the neurological disorder, Guillain-Barre syndrome (GBS), exhibit mimicry of gangliosides. Cross-reactive antibodies between C. jejuni LPS and gangliosides are considered to play an important role in GBS pathogenesis. In contrast, the O-chain of a number of Helicobacter pylori strains exhibit mimicry of Lewis(x) and Lewis(y) blood group antigens. The role of this mimicry may play a role in bacterial camouflage, the induction of autoimmunity and immune suppression in H. pylori-associated disease. ( Crit Rev Microbiol 1996;22(3):139-8 Preston A, Mandrell R E, Gibson B W, Apicella M A)

[0360] Bordetella, does not use molecular mimicry but has either LOS or LPS as a critical virulence factor. (Infect Immun 2000 Dec;68(12):6720 Harvill E T, Preston A, Cotter P A, Allen A G, Maskell D J, Miller J F). Bordetella pertussis, Bordetella parapertussis, and Bordetella bronchiseptica are closely related subspecies that cause respiratory tract infections in humans and other mammals and express many similar virulence factors. Therefore, a ligand (e.g. modulator) of the invention may be used in preventing or treating diseases associated with Bordetella.

[0361] The following non-limiting examples are illustrative of the present invention:

EXAMPLES Example 1

[0362] Material and Methods

[0363] Expression and Purification:

[0364] Recombinant LgtC-25 was over expressed in E. coli (AD202) as described previously (ref. 6). Briefly, the protein was first purified on a Q-sepharose fast flow column followed by a Superdex200 column (Pharmacia). Selenomethionyl LgtC was expressed in E. coli BL21 in minimal media supplemented with glucose and MgCl₂. When the cultures reached OD₆₀₀=0.6, selenomethionine (50 mg 1⁻¹) was added and at the same time the synthesis of methionine was down-regulated by the addition of 100 mg 1⁻¹ phenylalanine, threonine, lysine and 50 mg 1⁻¹ leucine, isoleucine, valine and proline (ref 41). After an additional 15 minutes, expression was induced with 0.5 mM IPTG after which the culture was grown for 6 hours. Selenomethionyl protein was purified following the same protocol with the exception that 5 mM DTT was included in all buffers. Incorporation of selenomethionine was confirmed by mass spectrometry. The structure was determined using a double cysteine mutant C128/174S from which more reproducible crystals could be produced than from the wildtype.

[0365] Site-directed Mutagenesis Via PCR.

[0366] All mutations were constructed in pCWlgtC-25 (ref. 6). A two stage PCR mutagenesis protocol was used. Two separate PCR reactions were performed, to generate two overlapping gene fragments, one of which contains the mutation. The primers were from the 5′ (primer 1) and (primer 2) 3′ ends of the gene as well as two internal primers. One internal primer contained the mutation and the other was chosen such that the 2 PCR products would overlap by 100 bp. These two products were gel purified, and then used as template for a third PCR reaction containing primers 1 and 2. This produced the fall length version of the gene with the mutation incorporated. Primers 1 and 2 contain BamHI and HindIII restriction sites which were used to subclone the final PCR product into pCW. Constructs were sequenced to verify the presence of only the mutation of interest.

[0367] Kinetic Assays

[0368] Synthesis of UDP-2Fgal was achieved essentially as described previously (ref. 19). Syntheses of 4′-deoxylactose, 6′-deoxylactose and galactosyl β-1,6-lactose will be described elsewhere. Kinetic studies were performed at 30° C. in 20 mM HEPES, pH 7.5 containing 0.1% bovine serum albumin, 50 mM KCl, 5 mM MnCl₂ and 5 mM DTT. The reaction was monitored via a continuous coupled assay similar to that described by Gosselin et al (ref. 42), in which UDP release is coupled to the oxidation of NADH (λ=340 nm, ε=6.22 nM⁻¹cm⁻¹). The change in absorbance was measured by means of a UNICAM 8700 UV-Vis spectrophotometer equipped with a circulating water bath. Kinetic parameters were calculated by direct fit of the initial rates to the respective equations using Grafit version 3.0 (ref.43).

[0369] Crystallization and Data Collection:

[0370] For crystallization 3 mM TCEP, 3 mM MnCl₂ and 5 mM UDP-2FGal was added to the protein (10 mg ml⁻¹) in 50 mM NH₄OAc, pH 7.0. The protein solution was further mixed in equal amounts with reservoir solution containing 50 mM NaOAc pH 5.0 and 5-20% PEG monomethylether 2000 and incubated on ice for 30 min before the solution was spun. Drops (6 μl) were allowed to equilibrate against the well solution as hanging drops and were streak seeded to induce crystallization. Orthorhombic LgtC crystals grow within a few hours of seeding and contain one molecule in the asymmetric unit (V_(M)=2.0 Å³ Da⁻¹) in space group P2₁2₁2₁ with unit cell dimensions a=39.79 Å b=76.05 Å c=86.84 Å.

[0371] A 2.0 Å MAD dataset, using four wavelengths, was collected at the Stanford Synchrotron Radiation Laboratory, beamline 1-5 using a Quantum Q4 CCD detector. For the deoxylactose complex, selenomethionyl crystals were soaked in 10 mM 4′-deoxylactose for 24 hours prior to data collection. Data were collected on a local Rigaka RU200 rotation anode equipped with OSMIC mirrors. All data were collected at 100K using mother liquor supplemented with 20% PEG 400 as cryoprotectant. All data was processed with DENZO and SCALEPACK (ref. 44). Statistics for data collection and processing are summarized in Table 2.

[0372] Structure Determination and Refinement:

[0373] The seven Se atom positions were determined using SOLVE (ref. 45). Phases and electron density maps were improved with DM (ref. 46). The initial density maps were of excellent quality and the model was easily built using XTALVIEW (ref. 47). The sequence differs from the published sequence (p96945) in three positions; an additional Gly was added at position 57, Ser 248 was exchanged for Pro and Gly 268 exchanged for Ala. These sequence differences were confirmed with DNA sequencing. The LgtC structure (with solvent, Mn and UDP-Gal removed) was used as the starting model for the 4-deoxylactose complex. Both complexes were refined with CNS 1.0 (ref. 48) where 5% of the data were flagged for the Rfree calculation. The parameters described by Engh and Huber (ref. 49) were used and the dictionaries for the substrates were generated by XPLO2D (ref. 50). All model building was performed using XTALVIEW. The quality of the models was analyzed with the program PROCHECK (ref. 51). Details of the refinement statistics are given in Table 2. Two regions with weak or no density have been excluded from the model, residues 218-221 between helix K and L, and the four C-terminal residues.

[0374] Structural Analysis and Figure Preparation:

[0375] Surfaces were calculated with the CCP4 program AREAIMOL using a probe with a 1.4 Å radius . (ref. 34). Superpositions were done with the program TOP (ref. 18). FIGS. 1 and 6 were prepared with ChemDraw; FIGS. 3, 4c and 5 were prepared with MOLSCRIPT52 and rendered with Raster3D 53. FIG. 4b was prepared with GRASP (ref 54).

[0376] Results and Discussion

[0377] Overall Fold:

[0378] The galactosyl transferase structure determined here is that of a deletion mutant of LgtC missing the C-terminal 25 residues. This was necessary since the C-terminal 50 residues of LgtC have been proposed to be involved in attachment of LgtC (and other related sugar transferases) to the surface of the bacterial membrane (ref. 6), and the full length protein is less stable. As shown in FIG. 2 the deleted part of the enzyme is very rich in basic residues (Arg 287, Lys 292, Arg 293, Arg 297, Arg 299, Arg 300, Lys 301, Arg 305, Arg 308, Lys 309) which would be complementary to the negatively charged phospholipids in the membrane. There are also several hydrophobic and aromatic residues (Ala 283, Val 284, Met 288, Phe 289, Met 294, Leu 295, Trp 298. Leu 302, Ala 304, Phe 306, Leu 307, Ile 310, Tyr 311), which suggests that the C-terminus associates with the membrane via hydrophobic as well as electrostatic interactions. A sequence alignment of seven bacterial enzymes, all belonging to glycosyltransferase family 8, reveals that they are relatively conserved in terms of sequence and size in both the substrate binding and membrane association domains (FIG. 2). It was also necessary to replace several cysteine residues that were believed to be responsible for (reversible) aggregation of the protein in order to produce a protein that crystallized. X-ray quality crystals were then produced reliably only in the presence of an inert analogue of the sugar donor, namely UDP 2-deoxy-2-fluoro-α-D-galactopyranose (UDP-2FGal).

[0379] The structure determined is that of a monomer comprising 286 residues that form a large N-terminal α/β domain which contains the active site and a smaller helical C-terminal domain which mediates membrane attachment The overall fold is presented in FIG. 3. A central β-sheet forms the core of the α/β-domain. The sheet contains seven strands (β3, β2, β1, β4, β7, β6, β8) all of which are parallel with the exception of β7. The first 100 residues provide a nucleotide binding fold composed of four parallel strands. sandwiched between helices A and B on one side and helices C and D on the other. Helix C and the N-terminal part of helix D are both of 3₁₀ character. The remainder of the central β-sheet is flanked by four α-helices on each side. In addition, an antiparallel β-ribbon formed by β5 and β9 lies almost perpendicular to the sheet The substrate binding cleft is an extended, largely occluded groove that lies along the base of the central β-sheet.

[0380] The small C-terminal domain of LgtC, residues 248-282 (the last four residues are disordered), is mainly helical, with helix M and helix N (which is 3₁₀ in nature) forming a small pedestal that packs perpendicular to helices A and B of the nucleotide binding motif and to the β-ribbon (FIG. 3c).

[0381] A structural homology search using the TOP server (ref. 18) indicates that only the N-terminal nucleotide binding motif of LgtC shares significant structural similarity with other protein structures in the PDB. The remaining segment, residues 101-282, displays limited identity with other known folds. The top hit is the inverting glycosyltransferase bovine β-1,4-galactosyltransferase (ref. 14). Despite the low sequence identity (˜14%), superposition of the structure of this enzyme with that of LgtC yields a root mean square (rms) deviation of 2.1 Å on 83 common C-α atoms (with portions of elements β1,2,3,4,5,7,8 and helices A, D, H, J, K and M having the closest similarity). The glycosyl transferase SpsA from Bacillus subtilis (ref. 13) also has some structural similarity with LgtC (rms deviation of 2.1 Å on 76 common C-α atoms with portions of elements β1,2,3,5,7,9 and helices A, C, D, J and L having the closest similarity). A significant difference between LgtC and the inverting transferases (SpsA, B4G and phage T4-transferase) is that the donor UDP-Gal is bound in a much more shallow, solvent-exposed binding cleft in comparison to the deep, solvent-shielded cleft of LgtC. This may well reflect a greater need to exclude solvent from the active site of an enzyme that forms a reactive glycosyl-enzyme intermediate.

[0382] UDP-sugar Binding Mode

[0383] The structure of LgtC was solved in complex with Mn²⁺ and a non-cleavable analogue of the donor sugar, UDP-Gal in which the hydroxyl at the 2 position of the galactose has been substituted by a fluorine. The fluorine at the 2-position serves to inductively destabilize the oxacarbenium ion-like transition states for the reaction catalyzed, thereby slowing the reaction dramatically. Indeed linetic studies showed that no transfer occurs from UDP-2FGal, but that it acts as an excellent inhibitor, with a K_(i) value of 2 μM (competitive with respect to UDP-Gal) as compared to the K_(m) value of 18 μM measured for UDP-Gal (Table 1). This fluorine substitution approach has been used previously to dramatically slow reaction rates in studies on glycosidases and on the mechanistically analogous glycogen phosphorylase¹⁰ and indeed UDP-2FGal has been synthesized previously and shown to inhibit two other galactosyltransferases¹⁹.

[0384] Most of the interactions between the enzyme and the nucleotide are formed by residues located at the C-terminus of β1 and the N-terminus of helix A. Two loops, from opposite sides of the groove, fold over the UDP-2FGal as a tight lid (FIGS. 3b, 4). The first loop, residues 75-80, is a part of the nucleotide binding motif and connects helix C with helix D. The second loop consists of residues 246-251 and is also part of a hinge between the N-terminal and the C-terminal domain. In the UDP-2FGal complex, the conformations of these two loops are stabilized primarily by interactions with the donor substrate in conjunction with additional intramolecular van der Waals (Vdw) interactions observed between His 78 and Pro 248. The structure indicates that these loops would likely be disordered or would adopt alternative conformations in the absence of the donor UDP-sugar. This may explain the inability to crystallize LgtC in the absence of UDP-2FGal.

[0385] The UDP-2FGal is almost entirely buried by the enzyme, leaving only 10 Å² or 1.5% of the molecule exposed to solvent (FIG. 4b). The donor sugar is highly ordered (Table 2) and adopts an unusual folded conformation in which the UDP moiety is bound in an extended manner but the galactose tucks back under the phosphates such that the plane of the galactose ring is almost parallel to the plane of the diphosphate (FIGS. 3, 4, 5). In other UDP-Gal complexes in the PDB, (for example in UDP-galactose 4-epimerase (ref. 20)), the UDP-Gal (or UDP-Glc) are bound in fully extended forms. As a measure of this conformation, a torsion angle calculated on PA and PB of the diphosphate and C1′ and C4′ of the galactose ring in LgtC is −10° compared to −160° in the epimerase structure. Interestingly, the conformation of the galactose-1-phosphate portion of the molecule is quite reminiscent of the conformation of glucose-1-phosphate or its analogues bound to glycogen phosphorylase (ref. 21). This is possibly quite relevant since glycogen phosphorylase is also a retaining glycosyltransferase.

[0386] The uridine diphosphate portion of UDP-2FGal binds in a cleft at the C-terminal end of the β-sheet while the uracil base stacks with conserved Tyr 11 (Phe in E. coli and Salmonella). The uracil carbonyl O4 forms a hydrogen bond with the ND2 group of Asn 10 while N3 of the base donates a hydrogen bond to OD1 of Asp 8. O2 of uracil is also within hydrogen bonding distance of the main chain nitrogen atom of Asp 8. The ribose ring adopts a C3-endo conformation in which 02 interacts with the carbonyl oxygen of Ala 6 and O3 with the main chain amide of Ile104. Both phosphates form hydrogen bonds with the protein, O2A with conserved Lys 250 (NZ) and O2B with Gly 247 (N) and His 78 (NE2).

[0387] The galactosyl moiety of the donor sugar is highly ordered within the LgtC active site (Table 2). The ring adopts a standard ⁴C₁ chair conformation similar to that of other UDP-galactose molecules in the PDB. O3′ forms hydrogen bonds to the side chain atoms of the invariant residues Asp 103 and Arg 86. O4′ and O6′ both hydrogen bond with the side chain carboxylate of the conserved Asp 188 indicating an important role for this residue in binding and probably in catalysis also. Such bidentate hydrogen bonding of a carboxyl group with vicinal hydroxyl groups on an active site sugar is well known, as in cyclodextrin glycosyltransferases and α-amylases (both family 13 ‘hydrolases’) where an aspartic acid residue bridges O2 and O3 of the substrate (ref. 22,23). F2 engages in only very weak interactions with a single active site residue (Asn 153), thereby possibly explaining why the binding constants of UDP-2Fgal and UDP-Gal are so similar. However, as a consequence of the folded conformation of the UDP-sugar, it engages in a relatively short interaction with an oxygen atom of the adjacent phosphate moiety. Presumably a hydroxyl group at the 2-position forms a hydrogen bond here, which likely becomes much stronger at the transition state as the glycosidic bond is cleaved and negative charge accumulates on the phosphate oxygens. This would stabilise the transition state, thus promoting catalysis. An additional hydrogen bond is formed between O6′ and the amide oxygen of the conserved Gln 189. There are also several Vdw interactions with the side chain atoms of Val 79, Thr 83, Gln 187 and Gln 189.

[0388] Manganese Binding

[0389] A “DXD” sequence motif is common to a wide range of glycosyltransferases, both in prokaryotes and eukaryotes, even though they may not share other sequence similarities (ref. 5,24,25). This motif has been proposed to be involved in the co-ordination of a divalent cation in the binding of the nucleotide sugar (ref. 26), though it may also show up in other contexts. Indeed, a number of mutagenesis studies have been carried out in various species on the conserved aspartate residues in the DXD sequence and all have found that enzymatic activity is completely abolished upon removal of the carboxylate, consistent with an important role in these cases (ref. 26-29). Interestingly, LgtC has four DXD motifs but only two are located within the active site of the enzyme. One is indeed shown to have important binding interactions with the metal ion while the role of the other is primarily in the binding of the acceptor sugar. Not surprisingly, these are also the only two served DXD motifs amongst the members of family 8. Based on these observations, it is clear that a DXD sequence is not always indicative of a metal binding site in glycosyltransferases and therefore should not be used as such. However, it is interesting to note that on the basis of the DXD sequence, an interesting glycosyltransferase activity was identified in the Fringe protein and this was shown to be responsible for modulating the activity of Notch receptors (ref. 30,31).

[0390] Earlier work has shown that manganese is required for enzyme stability and activity in LgtC, as in other related glycosyltransferases (ref. 6,32). It has been presumed that the metal functions to stabilize the UDP leaving group during bond cleavage. In the structure described herein, a single well-ordered Mn²⁺ ion is observed coordinated by the two phosphate oxygens of UDP as well as by the side chain atoms of three protein residues conserved throughout the family 8 glycosyltransferases, His 244, Asp 103 and Asp 105 (the latter two forming the DXD motif; FIG. 4). Asp 103 provides one liganding side-chain oxygen and Asp 105 provides a bidentate interaction. The co-ordination of the Mn²⁺ ion exhibits standard octahedral geometry with characteristic ligand distances ranging from 2.2 to 2.4 Å³³. Consistent with studies on DXD motifs in other systems, when Asp 103 is mutated to Asn or Glu activities drop dramatically, the k_(cat) values of the mutant being 2400-fold and 3500-fold lower compared to the wild type (Table 1). The bidentate ligand, Asp 105, is also essential for full activity; when substituted by Asn or Glu the mutated LgtC expresses very poorly.

[0391] Acceptor Binding:

[0392] The acceptor analog, 4-deoxylactose, in which the nucleophilic hydroxyl at the 4′ position has been replaced by hydrogen, cannot function as a substrate for LgtC, but does still act as an inhibitor K_(i)=16 mM with respect to lactose). Its binding is very similar to that of lactose (K_(m)=20 mM) indicating that interactions at the 4-position are not crucial for ground state binding. Highly ordered electron density for both donor and acceptor molecules is observed from data collected on LgtC/UDP-2FGal crystals into which the 4-deoxylactose was soaked. The non-reactive acceptor analogue is bound in a large open pocket on the C-terminal end of the α/β domain adjacent to the galactose moiety of the donor sugar. The pocket is formed by the loop between helices C and D, the domain hinge, helices F, I, J and K, (FIGS. 3, 4). The acceptor sugar is significantly more accessible to solvent than the donor, 141 Å² or 28% of the entire molecular surface. The non-reducing terminal galactose moiety of the lactose adopts a full chair conformation. A hydrogen bond is formed from O2 to a water molecule and from O6 to Asp 130 (OD2) and Gln 189 (NE2). Binding is also stabilised by Vdw interactions with the side chain atoms of Val 76, His 78, Tyr 186, Cys 246 and Gly 247. Mutation of Asp 130 to an alanine severely limits protein expression, perhaps reflecting the intricate structural role this amino acid plays, with hydrogen bonds to the side chain nitrogen of the conserved Asn 153 and to the main chain amide of Val 133 as well as to the lactose O6. A mutant Y186F, was also generated to address the possibility of a role for its OH group in binding or catalysis upon rotation of its side chain hydroxyl closer to the reactive centre. However, the mutation affects neither expression nor kinetic parameters (Table 1) suggesting that such an important role is unlikely though Vdw interactions of its ring atoms with the lactose are probably important.

[0393] The reducing end glucose moiety of the lactose also adopts a full chair conformation, binding of the ring being stabilized by hydrophobic stacking interactions with Phe 132 and Vdw interactions with the side chain atoms of Pro 211 and Pro 248 (FIGS. 4, 5). Hydrogen bonds from O3′ to the Thr 212 hydroxyl and main chain nitrogen (via a water molecule) and a direct hydrogen bond to the side chain of Cys 246 are also observed. Biochemical studies have shown that full LgtC activity is dependent on the presence of reducing agents (ref. 6). The structure described herein clearly shows that no cysteine residues are at a suitable distance from each other to form a disulfide bridge. However, the structure does suggest that oxidation of Cys 246, located on one of the two loops that envelop the donor sugar and within hydrogen bonding distance to the acceptor sugar, could result in impaired donor and acceptor binding.

[0394] The LgtC/UDP-2FGal structure is minimally changed upon acceptor binding (r.m.s of 0.16 Å on 282 C-α atoms). All hydrogen bonds between the donor and the enzyme are maintained, with additional bonds observed from O2A of the phosphate, to Tyr 11 (OH) and the carbonyl of His 78 via a water molecule. Furthermore, in the donor/acceptor complex, the side chain of Cys 246 adopts a new conformation to form a hydrogen bond with the lactose O3′ atom. In the LgtC/UDP-2FGal complex an acetate ion is bound between sp 130 and Gln 189. Upon acceptor binding the acetate is displaced by the deoxylactose with the O6 atom forming hydrogen bonds to the side chain carboxylate of Asp 130 and the side chain amide of Gln 189.

[0395] Implications for Catalysis:

[0396] LgtC has been shown to follow an ordered bi-bi kinetic mechanism in which UDP-Gal binds first, followed by lactose. Bond rearrangement then occurs and product trisaccharide is released first, followed by UDP. The structure determined is completely consistent with this mechanism since the UDP-2Fgal is deeply buried by two loops that fold over the active site. Acceptor sugar is not required to form this complex, and indeed no significant changes in the structure of this complex are seen upon binding of 4-deoxylactose. Importantly the 2-fluorogalactose moiety is highly ordered, with multiple hydrogen bonds and Vdw interactions from conserved active site residues. Although the order of Mn²⁺ binding has not been determined kinetically in this enzyme, the structure suggests that the metal ion remains bound to the protein throughout, consistent with the fact that addition of exogenous Mn²⁺ is not essential for catalysis. Its location in the active site, coordinating to oxygens of the α- and β-phosphate moieties of UDP-2Fgal, is typical, and is consistent with a role of the cation as an acid catalyst.

[0397] Efficient catalysis of galactosyl transfer requires that water be excluded from the active site, or at least carefully controlled therein, in order to ensure that hydrolysis does not occur. The close packing and occluded nature of the donor sugar in the LgtC structure limits the binding of ordered water molecules in the active site (FIG. 4b). In the UDP-2Fgal structure, only a single water molecule is within 5 Å of the reactive center C1′ of the donor galactose (4.4 Å) and this water is displaced by the O2 hydroxyl of deoxylactose upon formation of the ternary complex. Within this complex, the reactive center C1′ atom is entirely buried by residues Ile 76, Asp 103, Asp 130, Asp 153, Ala 154, Gly 155, Tyr 186, Gln 189, His 244, Cys 246, Gly 247 and by the acceptor sugar (as calculated with CONTACT³⁴ using a 6 Å cutoff). The closest water molecule in this complex is 7.3 Å away from the anomeric C1′ atom. Thus the enzyme has apparently evolved to exclude water, as would be expected.

[0398] As noted earlier, the stereochemical outcome of the reaction catalyzed suggests, by analogy with retaining glycosidases, that a double-displacement mechanism via a glycosyl-enzyme intermediate is occurring. If this is indeed true, then a suitable nucleophile should be located close to the anomeric carbon (C1′) of the UDP-2Fgal, and on the correct (β) face to allow direct displacement of the UDP leaving group.

[0399] Analysis of the LgtC structure indicates that the only polar atoms within 5 Å of the reactive center C1′ come from either the acceptor sugar (the lactose hydroxyl O3 (3.2 Å) and hydroxymethyl O6 (4.6 Å)) or from the side chain oxygen atom of Gln 189 (3.5 Å), and the side chain nitrogen atom of Asn 153 (4.2 Å). However, of these only the lactose O6 and the side chain oxygen atom of Gln 189 are located on the β-face on a reasonable trajectory. In light of experience with retaining glycosidases, this is surprising, since the carboxylate side chain of an Asp or Glu residue might have been anticipated on that basis. The two choices were therefore considered and evaluated separately, as follows.

[0400] The possibility of the 6-hydroxyl of lactose functioning in this fashion was initially intriguing, as this would have involved the enzyme first forming a tightly bound intermediate galactosyl β-1,6-lactose species. After movement away of the released UDP the 4-hydroxyl of the lactose could then attack the anomeric center from the α-face, forming the desired Gal α-1,4-lactose product (FIG. 6a). A particularly attractive component of this mechanism is the fact that it inherently demands formation of a ternary complex prior to the generation of a reactive intermediate, thereby minimizing the possibility of unwanted hydrolysis. Less attractive is the fact that the intermediate would not itself be inherently reactive, being a simple glycoside. The mechanism was probed experimentally in two ways. Firstly 6-deoxylactose, in which the putatively nucleophilic 6-hydroxyl had been removed, was synthesized and shown not to function as a substrate, which would be consistent with this mechanism. However, neither did it act as an inhibitor, thereby rendering its inactivity as a substrate meaningless. It does, however, indicate that binding interactions at that position, probably primarily with Asp 130, are quite important. More definitive results suggesting that this was not the likely mechanism come from the finding that galactosyl β-1,6-lactose, synthesized chemically, does not function as a substrate when incubated with LgtC in the presence of UDP plus the usual buffer components. Therefore, unless binding of this potential intermediate is too slow to permit measurable turnover, this mechanism is unlikely.

[0401] The alternative mechanism, in which the oxygen of Gln 189 attacks at the anomeric center to form an imidic ester intermediate (FIG. 6b) is initially unattractive given the fact that amides are notoriously poor nucleophiles. However, the reaction is entirely precedented, even within the field of glycosidases, since a chemically equivalent intermediate has been demonstrated to form during catalysis by N-acetylhexosaminidases from glycosidase families 18 and 20 (see ref. 10,11 for reviews). In those cases the substrate's own amide functionality attacks to form an oxazolinium ion intermediate (FIG. 6c) that is charge stabilized by an invariant carboxylate side chain close to the substrate nitrogen atom. In LgtC the oxygen atom of the side chain amide is well-positioned to perform a nucleophilic attack on C1′ both in terms of distance (3.5 Å) and in terms of the direction and angle of attack: the Cδ-Oε1-C1′ angle is 106.2° in good agreement with ideal values (FIG. 4c)³⁵. This identical position is seen in the complex with UDP-2Fgal (r.m.s of 0.14 Å on the 9 atoms of the residue), as might be expected for a pre-organised nucleophile. Gln 189 is contained within the invariant D/EQD motif (Helix J) found in all family 8 retaining glycosyltransferases (FIG. 3) (ref. 5). The side chain amide of Glnl 89 is fully buried in the donor/acceptor complex, and is oriented through several hydrogen bonds to both sugar (donation of a hydrogen bond from Nε1 to O6 of the lactose) and conserved protein side chains (acceptance of a hydrogen bond from the side chain Nε2 of Asn 153 (itself an invariant residue found within the NAG motif in all family 8 glycosyltransferases) and the main-chain NH of Ala 154, FIG. 4c). Furthermore, charge stabilization could be provided by the nearby (4.0 Å) carboxylate side chain of Asp 130.

[0402] Interestingly a mechanism of this type has been hinted at previously for another glycosyltransferase, glycogen phosphorylase, on the basis of structures of complexes with a suspected transition state analogue inhibitor, deoxynojirimycin tetrazole (ref. 36), and of a ternary complex with a thiooligosaccharide plus phosphate (ref. 37). In both cases the group identified as being closest to the anomeric center of the sugar to be transferred, and in the best position to function as catalytic nucleophile, is the main chain oxygen of the backbone amide of His 377. Similar to LgtC, stabilization of the developing positive charge on the nitrogen in this case can be afforded by the nearby aspartate (Asp 307) located within 4 Å of the amide nitrogen. Given the parallels in the reaction catalysed and the similarity in 3-dimensional structure with other transferases (ref. 38,39) this could indicate similar roles for these two amide carbonyl groups of LgtC and glycogen phosphorylase.

[0403] This mechanistic hypothesis was tested in LgtC through mutagenesis and kinetic analysis of the resultant mutants. The mutant Q189A has a k_(cat) value equaling 3% of that of the wild type enzyme (based on k_(cat) values measured with varying UDP-Gal), and a very similar K_(m) value for UDP-Gal. Interestingly, the K_(m) value for lactose was considerably (6-7 fold) higher than that for the wild type enzyme, consistent with the presence of a hydrogen bond between Nε₁ of Gln 189 and 06 of lactose. Importantly this confirms that the activity measured is indeed that of the mutant, and not due to contaminating wild type enzyme (itself unlikely since considerable precautions were taking during purification, including the use of new column packing materials for purification of this mutant). However, this relatively high residual activity renders a role for Gln 189 as the catalytic nucleophile somewhat unlikely given the presumed crucial importance of such a residue. Indeed, equivalent mutations of catalytic nucleophiles in retaining glycosidases typically reduce k_(cat) values by at least 10⁵ fold (ref. 10,11). The possibility that the mutant catalyses hydrolysis rather than transfer as a consequence of water binding in the site vacated by the side chain of Gln 189 was evaluated by product analysis. Only transfer products were observed, not galactose. Possible ‘rescue’ of activity by added small molecules that could bind in the cavity created, as has been seen for retaining glycosidases (ref. 11,40) was also probed. No rate increases were observed with any of the added reagents (formate, acetate, formamide, azide, acetamide), although modeling suggests that binding of these molecules in the Q189A mutation may be sterically unfavorable. Another possibility that cannot be ruled out is that an adjacent residue substitutes for Gln 189 within this mutant, but with lower efficiency.

[0404] Given the fact that definitive evidence of a double displacement mechanism remains elusive, a third possibility, but one with only limited chemical precedent, is that the reaction proceeds via a front side S_(N)2-like attack, otherwise known as an S_(N)i mechanism. In this scenario, approach of the nucleophile (the reactive hydroxyl of the acceptor sugar) towards the reactive centre would occur from the same side from which the UDP leaving group would depart and reaction would most likely proceed via a highly dissociative (oxocarbenium ion-like) transition state. Such a mechanism has been proposed previously for glycogen phosphorylase (ref. 9), but no experimental support has yet been accumulated.

[0405] Conclusions:

[0406] Determination of this first three-dimensional structure of a retaining nucleotide sugar-dependent glycosyl transferase in a complex with analogues of both substrates for the enzyme provides unique insights into the structure and mechanism of this important class of enzymes. Partial commonality of fold with those of several inverting transferases suggest that common structural elements are employed in the construction of a glycosyl transfer site, irrespective of the stereochemical outcome of the reaction.

[0407] This is the first structure of a glycosyltransferase to provide any structural information about the donor and acceptor sugars, and the first crystal structure of a retaining transferase, and is invaluable for rational inhibitor design.

Example 2

[0408] Synthesis of Alternate Acceptor Substrates:

[0409] 2,2′,3,3′,4′,6,6′-Hepta-O-acetyl-α-lactosyl Bromide (1)

[0410] To a 0° C. solution of per-O-acetylated β-D-lactose (4.7 g, 6.87 mmol) in anhydrous CH₂Cl₂ (15 mL) under nitrogen was added 45% HBr/AcOH (5.3 mL). The reaction vessel was then sealed and the solution was allowed to stir at room temperature. After 2.5 h, the reaction mixture was poured into chilled water (80 mL) and diluted with CH₂Cl₂ (60 mL). Solid NaHCO₃ was added to neutralize the excess acid and the layers were separated. The aqueous layer was further extracted with CH₂Cl₂ (2×80 mL) and the combined organic extracts were washed with water (2×80 mL), aq. NaHCO₃ (50 mL) and brine (50 mL). Evaporation of the solvent under reduced pressure after drying over MgSO₄ yielded 1 (4.5 g, 93%) as a white brittle solid. ¹H NMR (CDCl₃, 400 MHz): δ 6.5 (d, 1 H, J_(1,2) 4.0 Hz, H-1), 5.53 (dd, 1 H, J_(3,2) 9.6, J_(3,4) 9.6 Hz, H-3), 5.33 (dd, 1 H, J_(4′,3′) 3.4, J_(4′,5′) 0.9 Hz, H-4′), 5.11 (dd, 1 H, J_(2′,3′) 10.4, J_(2′,1′) 7.9 Hz, H-2′), 4.94 (dd, 1 H, J_(3′,2′) 10.4, J_(3′3,4′)3.4 Hz, H-3′), 4.74 (dd, 1 H, J_(2,3) 9.6, J _(2,1) 4.0 Hz, H-2), 4.49 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.47 (dd, 1 H, J_(6a,6b) 12.0, J_(6a,5) 1.7 Hz, H-6a), 4.02-4.23 (m, 4 H, H-5, H-6b, H-6a′, H-6b′), 3.86 (ddd, 1 H, J_(5′,6b′) 7.3, J_(5′,6a′) 6.4, J_(5′,4′) 0.9 Hz, H-5′), 3.83 (dd, 1 H, J_(4,5) 9.8, J_(4,3) 9.6 Hz, H-4), 2.13, 2.10, 2.06, 2.04, 2.03, 2.02, 1.94 (s, 21 H, 7×OAc).

[0411] Benzyl 2,2′,3,3′,4′,6,6′-hepta-O-acetyl-β-lactoside (2)

[0412] 1 (2.6 g, 3.69 mmol) was stirred in anhydrous CH₂Cl₂ (25 mL) containing 4 Å sieves under an atmosphere of nitrogen when benzyl alcohol (1.9 mL, 18.47 mmol) and AgCO₃ (2.0 g, 7.39 mmol) were added, along with a crystal of iodine. The reaction mixture was covered and stirred at room temperature overnight before it was filtered through Celite®. The filtrate was evaporated in vacuo and the residue was chromatographed over silica gel (PE:EtOAc, 3:2 to 1:1). Crystallization from PE/EtOAc yielded 2 (2.0 g, 75%) as a white solid. ¹H NMR (CDCl₃, 400 MHz): δ 7.22-7.35 (m, 5H, Ar), 5.32 (dd, 1 H, J_(4′,3′) 3.3, J_(4′,5′) 0.8 Hz, H-4′), 5.16 (dd, 1 H, J_(3,2) 9.3, J_(3,4) 9.2 Hz, H-3), 5.08 (dd, 1 H, J_(2′,3′) 10.4, J_(2′,1′) 7.9 Hz, H-2′), 4.99 (dd, 1 H, J_(2,3) 9.3, J_(2,1) 7.9 Hz, H-2), 4.93 (dd, 1 H, J_(3′,2′) 10.4, J_(3′,4′) 3.3 Hz, H-3′), 4.86 (d, 1 H, J 12.3 Hz, PhCH), 4.58 (d, 1 H, J 12.3 Hz, PhCH), 4.50 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.48 (d, 1 H, J_(1,2) 7.9 Hz, H-1), 4.48-4.52 (m, 1 H, H-6a), 4.00-4.15 (m, 3 H, H-6b, H-6a′, H-6b′), 3.84 (ddd, 1 H, J_(5′,6b′) 7.4, J_(5′,6a′) 6.3, J_(5′,4′) 0.8 Hz, h-5′), 3.79 (dd, 1 H, J_(4,5) 9.6, J _(4,3) 9.2 Hz, H-4), 3.56 (ddd, 1 H, J_(5,4) 9.6, J_(5,6b) 5.0, J_(5,6a) 2.0 Hz, H-5), 2.12, 2.11, 2.02, 2.01, 2.00, 1.98, 1.94 (s, 21H, 7×OAc).

[0413] Anal. Calcd. for C₃₃H₄₂O₁₈: C, 54.54; H, 5.83. Found: C, 54.50; H, 5.93.

[0414] Benzyl β-lactoside (3)

[0415] To a solution of 2 (1.24 g, 1.71 mmol) in anhydrous MeOH (30 mL) under nitrogen was added a catalytic amount of sodium methoxide until the pH of the solution was around 10. The reaction mixture was then stirred overnight at room temperature before it was neutralized with acidic Amberlyte® resin. After evaporation of the solvent, crystallization of the resulting residue from MeOH/EtOAc yielded 3 (0.64 g, 87%) as a white solid. ¹H NMR (D₂O, 400 MHz) selected data only: δ 7.30-7.60 (m, 5 H, Ar), 4.90 (d, 1 H, J 11.4 Hz, PhCH), 4.52 (d, 1 H, J_(1′,2′) 8.0 Hz, H-1′), 4.41 (d, 1 H, J_(1,2) 7.8 Hz, H-1), 3.95 (dd, 1 H, J_(6a,6b) 12.3, J_(6a,5) 2.1 Hz; H-6a), 3.88 (d, 1 H, J_(4′,3′) 3.3 Hz, H-4′), 3.32 (dd, 1 H, J_(4,5) 8.7, J_(4,3) 8.4 Hz, H-4).

[0416] Anal. Calcd. for C₁₉H₂₈O₁₁: C, 52.77; H, 6.53. Found: C, 52.47; H, 6.63.

[0417] Allyl 2,2′,3,3′,4′, 6,6′-hepta-O-acetyl-β-lactoside (4)

[0418] 1 (0.5 g, 0.69 mmol) was stirred in anhydrous CH₂Cl₂ (5 mL) containing 4 Å sieves under an atmosphere of nitrogen when allyl alcohol (0.24 mL, 3.46 mmol) and Ag2CO₃ (0.4 g, 1.38 mmol) were added along with a crystal of iodine. The reaction was covered and stirred at room temperature for 9 h before it was filtered through Celite®. The filtrate was evaporated in vacuo and the residue was chromatographed over silica gel (PE:EtOAc, 3:2 to 1: 1) to yield 4 (0.35 g, 76%) as a white solid. ¹H NMR (CDCl₃, 400 MHz): δ 5.81 (m, 1 H, OCH₂CH=CH₂), 5.32 (dd, 1 H, J_(4′,3′) 3.4, J _(4′,5′) 0.9 Hz, H-4′), 5.23 (ddd, 1 H, J_(trans) 17.3, J 3.2, J_(gem) 1.6 Hz, OCH₂CH=CH_(trans)), 5.17 (dd, 1 H, J_(3,2) 9.3, J_(3,4) 9.2 Hz, H-3), 5.17 (ddd, 1 H, J_(cis) 10.5, J 2.8, J_(gem) 1.6 Hz, OCH₂CH═CH_(cis)), 5.08 (dd, 1 H, J_(2′,3′) 10.4, J_(2′,1′) 7.9 Hz, H-2′), 4.93 (dd, 1 H, J_(3′,2′) 10.4, J_(3′,4′) 3.4 Hz, H-3′), 4.90 (dd, 1 H, J_(2,3) 9.3, J_(2,1) 7.9 Hz, H-2), 4.50 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.46 (d, 1 H, J_(1,2) 7.9 Hz, H-1), 4.44-4.50 (m, 1 H, H-6a), 4.27 (ddt, 1 H, J 13.2, J 4.9, J 1.5 Hz, OCR), 4.01-4.14 (m, 4 H, H-6b, H-6a′, H-6b′, OCH), 3.84 (ddd, 1 H, J_(5′,6b′) 7.2, J_(5′,6a′) 6.4, J_(5′,4′) 0.9 Hz, H-5′), 3.78 (dd, 1 H, J_(4,5) 9.7, J_(4,3) 9.2 Hz, H-4), 3.57 (ddd, 1 H, J_(5,4) 9.7, J_(5,6b) 5.0, J_(5,6a) 2.0 Hz, H-5), 2.13, 2.10, 2.03, 2.01, 1.94 (s, 21 H, 7×OAc).

[0419] Allyl β-lactoside (5)

[0420] 4 (0.14 g, 0.21 mmol) was dissolved in anhydrous MeOH at 0° C. under an atmosphere of nitrogen when gaseous ammonia was bubbled into the solution. After 5 min, both the ammonia source and ice bath were removed and the reaction mixture was stirred overnight at room temperature. Evaporation of the solvent in vacuo followed by chromatography over silica gel (EtOAc:MeOH:H₂O, 15:4:1) yielded 5 (47.5 mg, 60%) as a white solid. ¹H NMR (D₂O, 400 MHz) selected data only: δ 5.95 (m, 1 H, OCH₂CH═CH₂), 5.35 (dd, 1 H, J_(trans) 17.3, J_(gem) 1.4 Hz, CH═CH_(trans)), 5.26 (d, 1 H, J_(cis) 8.4 Hz, CH═CH_(cis)), 4.50 (d, 1 H, J_(1′,2′) 8.0 Hz, H-1′), 4.42 (d, 1 H, J_(1,2) 7.7 Hz, H-1), 4.37 (m, 1H, OCH), 4.20 (m, 1 H, OCH), 3.95 (dd, 1 H, J_(6a,6b) 12.2, J_(6a,5) 1.7 Hz, H-6a), 3.89 (d, 1 H, J_(4′,3′) 3.1 Hz, H-4′), 3.52 (dd, 1 H, J_(4,5) 9.8, J_(4,3) 7.8 Hz, H-4).

[0421] Anal. Calcd. for C₁₅H₂₆O₁₁.½H₂O: C, 46.03; H, 6.95. Found: C, 46.52; H, 6.85.

[0422] 4-Pentenyl 2,2′,3,3′,4′,6,6′-hepta-Oacetyl-β-lactoside (6)

[0423] 1 (0.5 g, 0.72 mmol) was stirred in anhydrous CH₂Cl₂ (5 mL) containing 4 Å sieves under an atmosphere of nitrogen when 4-penten-1-ol (0.37 mL, 3.60 mmol) and Hg(CN)₂ (0.3 g, 1.08 mmol) were added along with a crystal of iodine. The reaction mixture was covered and stirred at room temperature for 13.5 h before it was filtered through Celite®. The filtrate was evaporated in vacuo and the residue was chromatographed over silica gel (PE:EtOAc, 3:2 to 1:1) to yield 6 (0.21 g, 41%) as a colourless gum. ¹H NMR (CDCl₃, 400 MHz): δ 5.75 (m, 1 H, CH═CH,), 5.32 (dd, 1 H, J_(4′,3′) 3.4, J_(4′,5′) 0.8 Hz, H4′), 5.17 (dd, 1 H, J_(3,2) 9.4, J_(3,4) 9.2 Hz, H-3), 5.08 (dd, 1 H, J_(2′,3′) 10.4, J_(2′,1′) 7.9 Hz, H-2′), 4.98 (ddd, 1 H, J_(trans) 17.1, J 3.4, J_(gem) 1.7 Hz, CH═CH_(trans)), 4.93 (dd, 1 H, J_(3′,2′) 10.4, J_(3′,4′) 3.4 Hz, H-3′), 4.92-4.96 (m, 1 H, CH═CH_(cis)), 4.87 (dd, 1 H, J_(2,3) 9.4, J_(2,1) 8.0 Hz, H-2), 4.46 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.43 (d, 1 H, J_(1,2) 8.0 Hz, H-1), 4.42-4.46 (m, 1 H, H-6a), 4.02-4.14 (m, 3 H, H-6b, H-6a′, H-6b′), 3.87 (dd, 1 H, J_(4,5) 9.7, J_(4,3) 9.2 Hz, H4), 3.84 (m, 1 H, H-5′), 3.81 (dt, 1 H, J 9.8, J 6.2 Hz, OCH), 3.57 (ddd, 1 H, J_(5,4) 9.7, J_(5,6b) 5.1, J_(5,6a) 2.0 Hz, H-5), 3.45 (dt, 1 H, J 9.8, J6.7 Hz, OCH), 2.14,2.12, 2.09,2.03, 2.02, 2.01, 1.94 (s, 21 H, 7×OAc), 1.52-1.70 (m, 4 H, CH₂CH₂).

[0424] 4-Pentenyl β-lactoside (7)

[0425] To a solution of 6 (0.45 g, 0.63 mmol) in anhydrous MeOH (20 mL) under nitrogen was added a catalytic amount of sodium methoxide until the pH of the solution was around 10. The reaction mixture was then stirred overnight at room temperature before it was neutralized with acidic Amberlyte® resin. After the solvent was evaporated in vacuo, chromatography of the resulting residue over silica gel (EtOAc:MeOH:H₂O, 15:4:1) yielded 7 (0.17 g, 67%) as a white powder. ¹H NMR (D₂O, 400 MHz) selected data only: δ 5.89 (m, 1 H, CH═CH₂), 5.06 (dd, 1 H, J_(trans)17.3, J_(gem) 1.0 Hz, CH═CH_(trans)), 5.00 (dd, 1 H, J_(cis) 9.3, J_(gem) 1.0 Hz, CH═CH_(cis)), 4.45 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 4.42 (d, 1 H, J_(1,2) 7.6 Hz, H-1), 2.07-2.17 (m, 2 H, CH₂CH═CH₂), 1.65-1.75 (m, 2 H, OCH₂—CH₂).

[0426] Anal. Calcd. for C₁₇H₃₀O₁₁.½H₂O: C, 48.68; H, 7.45. Found: C, 48.98; H, 7.14.

[0427] 2,3-Dihydroxypropyl 2,2′,3,3′,4′,6,6′-hepta-O-acetyl-β-lactoside (8)

[0428] N-Methylmorpholino N-oxide (0.02 g, 0.18 mmol) was dissolved in a solution of 4:1 acetone:water (1.5 mL) under an atmosphere of nitrogen at 0° C. when a catalytic amount of osmium tetroxide in t-butanol was added. To this was added a solution of 4 (0.11 g, 0.16 mmol) in acetone (0.5 mL) and the reaction mixture was stirred overnight. Sodium bisulfite (0.06 g, 0.55 mmol) in water (1 mL) was then added to the reaction and stirring was continued for 1 h. The reaction was poured into brine (10 mL) and extracted with CH₂Cl₂ (2×10 mL). Evaporation of the combined organic layers after drying over MgSO₄ yielded 8 (0.11 g, 96%) as a white solid. ¹H NMR (CDCl₃, 400 MHz) selected data only: δ 5.35 (d, 1 H, J_(4′.,3′) 3.3 Hz, H-4′), 5.18 (dd, 1 H, J_(3,2) 9.5, J_(3,4) 9.1 HZ, H-3), 5.08 (dd, 1 H, J_(2′,3′) 10.4, J_(2′,1′) 7.9 Hz, H-2′), 4.94 (dd, 1 H, J_(3′,2′) 10.4, J_(3′,4′) 3.3 Hz, H-3′), 4.87 (dd, 1 H, J_(2,3) 9.5, J_(2,1) 8.0 Hz, H-2), 4.53 (ddd, 1 H, J 12.1, J 5.3, J 2.1 Hz, OCH), 4.44 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.42 (d, 1 H, J_(1,2) 8.0 Hz, H-1), 2.17, 2.13, 2.05, 2.03, 2.02, 1.94 (s, 21 H, 7×OAc).

[0429] 2,3-Dihydroxypropyl β-lactoside (9)

[0430] To a solution of 8 (0.10 g, 0.15 mmol) in anhydrous MeOH (20 mL) under nitrogen was added a catalytic amount of sodium methoxide until the pH of the solution was around 10. The reaction mixture was then stirred overnight at room temperature before it was neutralized with acidic Amberlyte® resin. After evaporation of the solvent, crystalization of the resulting residue from MeOH yielded 9 (34.5 mg, 57%) as a white solid. ¹H NMR (D₂O, 400 MHz) selected data only: δ 4.47 (d, 1 H, J_(1,2) 8.0 Hz, H-1), 4.42 (d, 1 H, J_(1′,2′) 8.0 Hz, H-1′).

[0431] Anal. Calcd. for C₁₅H₂₈O₁₃: C, 43.27; H, 6.78. Found: C, 43.30; H, 6.92.

[0432] Synthesis of UDP-2FGal:

[0433] 3,4,6-Tri-O-acetyl-2-deoxy-2-fluoro-D-galactopyranose (10)

[0434] 3,4,6-Tri-O-acetyl-D-galactal (0.912 g, 3.349 mmol) was dissolved in DMF (15 mL), then water (6 mL) and Selectfluor™ (N-fluoro-N-chloromethyltriethylenediamine bis(tetrafluoroborate), 4.20 g, 11.80 mmol) from Air Products and Chemicals Inc. were added and the reaction mixture was stirred at 50° C. After 24 h, the reaction was shown to be complete by TLC (PE:EtOAc, 3:2). To the reaction mixture was added water (40 mL) and this was then extracted with CH₂Cl₂ (3×50 mL). The combined organic layers were washed with water (3×50 mL), dried over MgSO₄ and the solvent was removed under reduced pressure. Chromatography of the resulting residue over silica gel (PE:EtOAc, 3:2 to 1: 1) yielded 10 (0.36 g, 35%) as a colourless gum. ¹H NMR (CDCl₃, 400 MHz) for the α anomer: δ 5.52 (d, 1 H, J_(1,2) 3.8 Hz, H-1), 5.38-5.50 (m, 2 H, H-3, H-4), 4.75 (ddd, 1 H, J_(2,F) 49.9, J_(2,3) 10.0, J_(2,1) 3.8 Hz, H-2), 4.47 (m, 1 H, H-5), 4.00-4.15 (m, 2 H H-6a, H-6b), 2.10, 2.00, 1.99 (s, 9 H, 3×OAc). ¹⁹FNMR(CDCl₃, 188 MHz): δ-131.1 (dd, J_(F,2) 49.9, J_(F,3) 14.5 Hz).

[0435] 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-fluoro-β-galactopyranose (11)

[0436] To a solution of 10 (0.88 g, 2.84 mmol) in pyridine (7 mL) was added acetic anhydride (3.5 mL) and the reaction was stirred at room temperature overnight The pyridine and acetic anhydride were then removed by evaporation under reduced pressure and the residue was then taken up in 10% v/v HCl (80 mL) and extracted with CH₂Cl₂ (3×70 mL). The combined organic extracts were washed with 10% v/v HCl (70 mL), aq. NaHCO₃ (70 mL), water (70 mL) and brine (70 mL), dried over MgSO₄ and the solvent was evaporated in vacuo to yield the desired compound as a mixture of anomers. The residue was then dissolved in anhydrous CH₂Cl₂ (10 mL) under an atmosphere of argon and the temperature was brought to 0° C. To this was added a solution of 45% HBr/AcOH after which the argon source was removed and the reaction vessel was sealed and allowed to warm to room temperature. After 4 h, the reaction was poured into ice water (80 mL) and diluted with CH₂Cl₂ (80 mL). Solid NaHCO₃ was added to neutralize the excess acid and the layers were separated. The aqueous layer was further extracted with CH₂Cl₂ (2×70 mL). The organic layers were subsequently combined and washed with aq. NaHCO₃ (2×70 mL), water (100 mL) and brine (70 mL) and dried over MgSO₄. Evaporation of the solvent under reduced pressure yielded a beige gum to which acetic acid (35 mL) and Hg(OAc)₂ (1.87 g, 5.97 mmol) were added. The reaction was allowed to stir at room temperature under an atmosphere of argon. After 3 h, the reaction was poured into water (100 mL) and then extracted with CH₂Cl₂ (3×80 mL). The combined organic extracts were washed with aq. NaHCO₃ (3×80 mL), water (80 mL) and brine (80 mL). After drying over MgSO₄, the solvent was removed in vacuo and the residue was chromatographed over silica gel (PE:EtOAc, 3:1 to 5:2) to yield 11 (0.83 g, 83%) as a white solid. ¹H NMR (CDCl₃, 400 MHz): δ 5.77 (dd, 1 H, J_(1,2) 8.1, J_(1,F) 4.1 Hz, H-1), 5.43 (m, 1 H, H-4), 5.15 (ddd, 1 H, J_(3,F) 13.2, J_(3,2) 9.8, J_(3,4) 3.6 Hz, H-3), 4.62 (ddd, 1H, J_(2,F) 51.6, J_(2,3) 9.8, J_(2,1) 8.1 Hz, H-2), 4.05-4.20 (m, 3 H, H-5, H-6a, H6b), 2.18, 2.14, 2.05, 2.03 (s, 12 H, 4×OAc). ¹⁹F NMR (CDCl₃, 188 MHz): δ-132.1 (ddd, J_(F,2) 51.6, J_(F,3) 13.2, J_(F,1) 4.1 Hz).

[0437] 2-Deoxy-2-fluoro-α-D-galactopyranose-1-phosphate, mono(tri-n-octyl)ammonium Salt (12)

[0438] Anhydrous H₃PO₄ (0.31 g, 3.17 mmol) was dried under vacuum for 24 h before it was melted at 50° C. 11 (0.14 g, 0.40 mmol) was then added and the reaction mixture was stirred under reduced pressure (20 mm Hg) for 9 h. After this time, THF (1 mL) and a solution of 2 M LiOH (6 mL) were added and the reaction mixture was allowed to stir at room temperature overnight After filtering through Celite® and washing with 0.01 M LiOH, the solvent was evaporated in vacuo. The residue was then dissolved in water and passed through a column of Bio-Rad AG 50W-X2, 200-400 mesh, sulfonic acid cation exchanger (H⁺ form). The desired fractions were pooled and the solvent volume was decreased by evaporation under reduced pressure. Tri-n-octylamine (0.14 g, 0.40 mmol) was added and the solution was lyophilized yielding 12 (0.28 g) as a colourless syrup. ¹H NMR (CDCl₃, 400 MHz): δ 5.74 (dd, 1 H, J_(1,P) 5-9, J_(1,2) 3.6 Hz, H-1), 4.63 (m, 1 H, H-2), 4.23 (m, 1 H, H-3), 3.72-4.15 (m, 4 H, H-4, H-5, H-6a, H-6b), 2.80 (m, 6 H, NCH₂), 1.65 (m, 6 H, NCCH₂), 1.30 (m, 30 H, CH₂), 0.85 (t, 9 H, CH₃). ¹⁹F NMR (CDCl₃, 188 MHz, proton decoupled): δ-132.4. ³¹P NMR (CDCl₃, 81 MHz proton decoupled): δ 0.01.

[0439] Uridine 5′-diphospho-(2-deoxy-2-fluoro)-α-D-galactopyranose, di-ammonium Salt (13)

[0440] To 12 (0.25 g, 0.40 mmol) was added anhydrous pyridine (5 mL) which was then evaporated. This procedure was repeated twice before UMP-morpholidate (0.33 g, 0.48 mmol) was added. Evaporation with anhydrous pyridine (5 mL) was again repeated three times. 1H tetrazole (0.07 g, 1.01 mmol) and anhydrous pyridine (3 mL) were then added and the reaction mixture was stirred at room temperature. An aliquot of the reaction mixture was transferred into an NMR tube containing a capillary of DMSO-d6 so that the progress of the reaction could be monitored via ³¹P NMR. After 27 days, the reaction mixture was diluted with water and evaporated under reduced pressure. After repeating this four times, the residue was taken up in 100 mM NH₄HCO₃ (5 mL) and the tri-n-octylamine was extracted with diethyl ether (3×5 mL). The aqueous layer was lyophilized to yield the crude product Purification was afforded by size exclusion chromatography through a column of Bio-Gel P2 extra fine resin (1×45 cm) using a Beckman Biosepra ProSys Workstation. The product was eluted with 250 mM NH₄HCO₃ at a flow rate of 0.1 mL/min. The desired fractions were pooled and lyophilized to yield 13 (90.0 mg, 37%) as a white powdery solid. ¹H NMR (D₂O, 400 MHz) selected data only: δ 7.91 (d, 1 H, J_(6,5) 6.1 HZ H-6), 5.93 (m, 2 H, H-1′, H5), 5.76 (dd, 1 H J_(1″,P) 7.1, J_(1″,2) 3.6, H-1″). ¹⁹F NMR (D₂O, 188 MHz): δ-132.4 (dd, J_(2″,F) 49.9, J^(3″,F) 11.1 Hz). ³¹P NMR (D₂O, 81 MHz, proton decoupled): δ-9.10 (d, JPβ,Pα 19.9 Hz, P^(β)), −10.8 (d, J_(Pα,Pβ) 19.9 Hz, P^(α)).

[0441] Anal. Calcd. for C₁₅H₂₉FN₄O₁₆P₂: C, 29.91; H, 4.85; N, 9.30. Found: C, 30.37; H, 5.34; N, 9.89.

[0442] Synthesis of Incompetent Acceptor Substrates:

[0443] 1,2,2′,3,3′,6-Hexa-O-acelyl-4′,6′-O-benzylidene-α-lactose (14)

[0444] To a suspension of lactose (45 g, 124.90 mmol) in DMF (110 mL) was added benzaldehyde dimethyl acetal (20.6 mL, 137.40 mmol) followed by a catalytic amount of p-toluenesulphonic acid (0.47 g, 2.5 mmol). The reaction mixture was then stirred under reduced pressure (20 mm Hg) for 4 d at 60° C. After this time, water (200 mL) was added and unreacted benzaldehyde dimethyl acetal was extracted with EtOAc (2×200 mL). The aqueous layer was evaporated in vacuo following which, pyridine (200 mL) and acetic anhydride (100 mL) were then added to the resulting residue. The reaction mixture was allowed to stir overnight before the volume was decreased by evaporation under reduced pressure. To the remaining residue was added ice water (300 mL) and the crude product was then extracted with CH₂Cl₂ (2×250 mL). The combined organic layers were washed with 10% v/v HCl (3×200 mL), water (2×200 mL) and brine (1×250 mL), dried over MgSO₄ and the solvent was evaporated under reduced pressure. Crystallization from EtOAc/Hexane yielded 14 as a slightly yellowish solid (8 g, 10%). ¹H NMR (CDCl₃, 200 MHz): δ 7.30-7.55 (m, 5 H, Ar), 6.45 (d, 1 H, J_(1,2) 3.7 Hz, H-1), 5.48 (s, 1 H, PhCH), 5.45 (dd, 1 H, J_(3,2) 10.4, J_(3,4) 9.9 Hz, H-3), 5.35 (dd, 1 H, J_(2′,3′) 10.3, J_(2′,1′) 7.9 Hz, H-2′), 5.05 (dd, 1 H, J_(2,3) 10.4, J_(2,1) 3.7 Hz, H-2), 4.87 (dd, 1 H, J_(3′,2′) 10.3, J_(3′,4′) 3.5 Hz, H-3′), 4.45 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.30-4.55 (m, 1 H, H-5), 4.15-4.45 (m, 2 H, H6a, H-6b), 4.13 (dd, 1 H, J_(6a′,6b′) 8.2, J_(6a′,5′) 4.1 Hz, H-6a′), 4.08 (dd, 1 H, J_(4′,3′) 3.5, J_(4′,5′) 1.6 Hz, H-4), 3.95-4.05 (m, 2 H, H-5′, H-6b′), 3.80 (dd, 1 H, J_(4,3) 9.9, J_(4,5) 9.3 Hz, H-4), 2.17, 2.11, 2.15, 2.14, 2.00 (s, 18 H, 6×OAc).

[0445] 1,2,2′,3,3′,6-Hexa-O-acetyl-6′-O-benzyl-α-lactose (15)

[0446] 14 (3.5 g, 5.13 mmol) was dissolved in anhydrous THF (120 mL) when sodium cyanoborohydride (3.2 g, 51.27 mmol) was added. A saturated solution of HCl in diethyl ether was then cannulated into the reaction mixture in portions until the evolution of gas had ceased. Within 0.5 h, the reaction was judged to be complete by TLC (PE:EtOAc, 1:1). At this time, the reaction mixture was added to water (100 mL) and the crude product was extracted with CH₂Cl₂ (2×100 mL). The combined organic layers were washed with aq NaHCO₃ (2×100 mL) and water (100 mL), dried over MgSO₄ and evaporated in vacuo. Chromatography over silica gel (PE:EtOAc, 4:5) yielded 15 as a white solid (2.66 g, 76%). ¹H NMR (CDCl₃, 200 MHz) selected data only: δ 7.30-7.45 (m, 5 H, Ar), 6.25 (d, 1 H, J_(1,2) 3.7 Hz, H-1), 5.43 (dd, 1 H, J_(3,2) 10.2, J_(3,4) 9.1 Hz, H-3), 5.19 (dd, 1 H, J_(2′,3′) 10.1, J_(2′,1′) 7.8 Hz, H-2′), 5.02 (dd, 1 H, J_(2,3) 10.2, J_(2,1) 3.7 Hz, H-2), 4.89 (dd, 1H, J_(3′,2′) 10.1, J_(3′,4′) 3.1 Hz, H-3′), 4.52 (s, 2 H, PhCH₂), 4.45 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 2.15, 2.10, 2.07, 2.04, 2.01,2.00 (s, 18 H, 6×OAc).

[0447] 1,2,2′,3,3′,6-Hexa-O-acetyl-6′-O-benzyl-4′-deoxy-4′-iodo-α-cellobiose (16)

[0448] A stirring solution of 15 (1.32 g, 1.93 mmol) in anhydrous CH₂Cl₂ (15 mL) under argon was cooled to −20° C. before pyridine (5 mL) and triflic anhydride (0.88 mL, 5.20 mmol) were added The reaction mixture was then warmed to room temperature and stirred for 2 h prior to the addition of aq NaHCO₃ (50 mL). The crude material was extracted with CH₂Cl₂ (2×35 mL) and the combined organic extracts were subsequently washed with water (2×80 mL). Coevaporation of the organic layer with MeCN under reduced pressure yielded a yellow foamy gum, which was then dissolved in anhydrous DMF (25 mL). After the addition of Nal (1.44 g, 9.63 mmol), the reaction mixture was allowed to stir at room temperature overnight under an atmosphere of argon before being added to aq NaHCO₃ (100 mL) and extracted with CH₂Cl₂ (3×125 mL). After the combined organic layers were washed with water (2×75 mL), dried over MgSO₄ and evaporated under reduced pressure, the resulting residue was crystallized from EtOAc/Hexane to yield 16 (0.94 g, 62%) as a cotton-like solid. ¹H NMR (CDCl₃, 200 MHz) selected data only: δ 7.30-7.45 (m, 5 H, Ar), 6.24 (d, 1 H, J_(1,2) 3.7 Hz, H-1), 5.42 (dd, 1 H, J_(3,2) 10.3, J_(3,4) 9.3 Hz, H-3), 5.25 (dd, 1 H, J_(3′,2′) 9.2, J_(3′,4′) 11.0 Hz, H-3′), 5.00 (dd, 1 H, J₂₃ 10.3, J_(2,1) 3.7 Hz, H-2), 4.78 (dd, 1 H, J_(2′,3′) 9.2, J_(2′,1′) 8.1 Hz, H-2′), 4.50 (s, 2 H, PhCH₂), 4.48 (d, 1 H, J_(1′,2′) 8.1 Hz, H-1′), 2.12,2.09,2.06,2.01, 2.00 (s, 18 H, 6×OAc).

[0449] 1,2,2′,3,3′,6-Hexa-O-acetyl-6′-O-benzyl-4′-deoxy-α-lactose (17)

[0450] To a solution of 16 (0.90 g, 1.13 mmol) in anhydrous benzene (30 mL) under argon was added tributyltin hydride (1.65 g, 5.67 mmol) and a catalytic amount of AIBN. The reaction mixture was then refluxed for 45 min after which time the solvent was evaporated in vacuo. The residue was dissolved in MeCN (120 mL) and washed with hexane (3×70 mL). Evaporation of the MeCN layer followed by crystallization from EtOAc/Hexane yielded 17 (0.87 g, 85%) as a white fluffy solid. ¹H NMR (CDCl₃, 400 MHz): δ 7.25-7.40 (m, S H, Ar), 6.24 (d, 1 H, J_(1,2) 3.7 Hz, H-1), 5.42 (dd, 1 H, J_(3,2) 10.1, J_(3,4) 9.4 H, H-3), 4.99 (dd, 1 H, J₂₃ 10.1, J_(2,1) 3.7 HZ, H-2), 4.91 (ddd, 1 H, J_(3′,4′ax) 11.3, J_(3′,2′) 9.6, J_(3′,4′eq) 5.4 Hz, H-3′), 4.80 (dd, 1 H, J_(2′,3′) 9.6, J_(2′,1′) 7.8 Hz, H-1′), 4.50 (s, 2 H, PhCH₂), 4.43 (dd, 1 H, J_(6a,6b) 12.2, J_(6a,5) 2.0 Hz, H-6a), 4.36 (d, 1 H, J_(1′,2+) 7.8 Hz, H-1′), 4.12 (dd, 1 H, J_(6b,6a) 12.2, J_(6b,5) 4.3 Hz, H-6b), 3.97 (ddd, 1 H, J_(5,4) 10.1, J_(5,6b) 4.3, J _(5,6a) 2.0 Hz, H-5), 3.78 (dd, 1 H, J_(4,5) 10.1, J_(4,3) 9.4 Hz, H-4), 3.60-3.67 (m, 1 H, H-5′), 3.56 (dd, 1 H, J_(6a′,6b′) 9.8, J_(6a′,5′) 5.3 Hz, H-6a′), 3.45 (dd, 1 H, J_(6b′,6a′) 9.8, J_(6b′,5′) 4.8 Hz, H-6b′), 2.14, 2.08, 2.01, 1.98 (s, 18 H, 6×OAc), 2.00-2.10 (m, 1 H, H4′_(eq)), 1.50-1.64 (m, 1 H, H-4′_(ax)).

[0451] 1,2,2′,3,3′,6-Hexa-O-acetyl-4′-deoxy-α-lactose (18)

[0452] 17 (0.23 g, 0.34 mmol) was dissolved in EtOH (4 mL) when cyclohexene (1.39 mL, 13.76 mmol) and 20% Pd(OH)₂/C (0.06 g) were added and the reaction mixture was refluxed. After 2 h, the catalyst was removed by filtration through Celite® and the filtrate was evaporated in vacuo. Crystallization from EtOH yielded 18 (0.13 g, 63%) as a white fluffy solid. ¹H NMR (CDCl₃, 400 MHz): δ 6.24 (d, 1 H, J_(1,2) 3.7 Hz, H-1), 5.45 (dd, 1 H, J_(3,2) 10.0, J_(3,4) 9.2 Hz, H-3), 5.01 (dd, 1 H, J_(2,3) 10.0, J_(2,1) 3.8 Hz, H-2), 4.94 (ddd, 1 H, J_(3′,4′ax) 11.5, J_(3′,2′) 9.5, J_(3′,4′eq) 5.4 Hz, H-3′), 4.81 (dd, 1 H, J_(2′,3′) 9.5, J_(2′,1′) 7.7 Hz, H-2′), 4.47 (d, 1 H, J_(1′,2′) 7.7 Hz, H-1′), 4.44 (dd, 1 H, J_(6a,6b) 12.5, J_(6a,5) 2.0 Hz, H-6a), 4.08 (dd, 1 H, J_(6b,6a) 12.5, J_(6b,5) 4.5 Hz, H-6b), 4.00 (ddd, 1 H, J_(5,4) 10.0, J_(5,6b) 4.5, J_(5,6a) 2.0 Hz, H-5), 3.83 (dd, 1 H, J_(4,5) 10.0, J_(4,3) 9.2 Hz, H-4), 3.52-3.68 (m, 3 H, H-5′, H-6a′, H-6b′), 2.15, 2.08, 2.06, 2.04, 1.98, 1.97 (s, 18 H, 6×OAc), 2.00-2.10 (m, 1 H, H-4′_(eq)), 1.50-1.64 (m, 1 H, H-4′_(ax)).

[0453] 4′-Deoxylactose (19)

[0454] To a stirring solution of 18 (0.50 g, 0.87 mmol) in anhydrous MeOH (8 mL) under argon was added a catalytic amount of sodium methoxide until the solution was slightly basic. The reaction mixture was allowed to stir at room temperature overnight prior to being neutralized with Amberlyte® IR-120 acidic resin. After filtration, evaporation of the solvent under reduced pressure yielded 19 (0.24 g, 85%) as a white solid. ¹H NMR (D₂O, 400 MHz) selected data only for β anomer: δ 4.63 (d, 1 H, J_(1,2) 8.0 Hz, H-1), 4.40 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 3.22-3.29 (m, 1 H, H-5), 3.19 (ddd, 1 H, J_(5′,4′ax) 11.2, J_(5′,6a′) 8.0, J_(5′,6b′) 3.2 Hz, H-5′), 1.95 (dd, 1 H, J_(4′eq,4′ax) 12.0, J_(4′eq,3′) 4.4 Hz, H-4′_(eq)), 1.42 (ddd, 1 H, J_(4′ax,4′eq) 12.0, J_(4′ax,3′) 11.9, J_(4′ax,5′) 11.2 Hz, H-4′_(ax)).

[0455] Anal. Calcd. for C₁₂H₂₂O₁₀: C, 44.17; H, 6.80. Found: C, 43.87; H, 6.91.

[0456] 2,2′,3,3′,4′,6,6′-Hepta-O-acetyl-α-cellobiosyl Bromide (20)

[0457] A solution of octa-O-acetylcellobiose (10.95 g, 16.10 mmol) in anhydrous CH₂Cl₂ (35 mL) under an atmosphere of nitrogen was cooled to 0° C. prior to the addition of 45% w/v HBr/AcOH (13 mL). The reaction vessel was then sealed and the reaction mixture was allowed to warm to room temperature. After 4 h, the reaction mixture was diluted with CH₂Cl₂ (100 mL) and the solution was added to ice water (200 mL) whereupon it was neutralized with solid NaHCO₃. Upon separation of the two phases, the aqueous layer was further extracted with CH₂Cl₂ (2×100 mL) and the combined organic extracts were washed with aq. NaHCO₃ (2×75 mL), water (75 mL) and brine (75 mL). Removal of the solvent under reduced pressure after drying over MgSO₄ yielded 20 as a white solid (11.12 g, 99%). ¹H NMR (CDCl₃, 400 MH): δ 6.50 (d, 1 H, J_(1,2) 4.1 Hz, H-1), 5.50 (dd, 1 H, J_(3,2) 9.7, J_(3,4) 9.7 Hz, H-3), 5.13 (dd, 1 H, J_(3′,4′) 9.3, J_(3′,2′) 9.2 Hz, H-3′), 5.05 (dd, 1 H, J_(4′,5′) 9.7, J_(4′,3′) 9.3 Hz, H-4′), 4.91 (dd, 1 H, J_(6a′,6b′) 12.5, J_(6a′,5′) 4.5 Hz, H-6a′), 4.11-4.23 (m, 2 H, H-5, H-6b), 4.03 (dd, 1 H, J_(6b′,6a′) 12.5, J_(6b′,5′) 2.3 Hz, H-6b′), 3.81 (dd, 1 H, J_(4,3) 9.7, J_(4,5) 9.7 Hz, H-4), 3.65 (ddd, 1 H, J_(5′,4′) 9.7, J_(5′,6a′) 4.5, J_(5′,6b′) 2.3 Hz, H-5′), 2.11, 2.06, 2.01, 2.00, 1.98, 1.96 (s,21 H, 7×OAc).

[0458] Benzyl 2,2′,3,3′,4′,6,6′-hepta-O-acetyl-β-cellobioside (21)

[0459] To a solution of 20 (9.99 g, 14.29 mmol) in anhydrous CH₂Cl₂ (100 mL) containing 4 Å molecular sieves under an atmosphere of nitrogen was added benzyl alcohol (7.39 mL, 71.44 mmol) and silver carbonate (7.88 g, 28.58 mmol). A crystal of iodine was added and the reaction vessel was shielded from the light and stirred at room temperature overnight After this time, the reaction mixture was filtered through Celite® and washed with CH₂Cl₂. The solvent was then evaporated in vacuo and the residue was crystallized from EtOAc/Hex to yield 21 (6.91 g, 66%) as a white fluffy solid. ¹H NMR (CDCl₃, 400 MHz): δ 7.20-7.35 (m, 5 H, Ar), 5.11 (dd, 2 H, J_(3,2/3′,2′) 9.3, J_(3,4/3′,4′) 9.3 Hz, H-3, H-3′), 5.03 (dd, 1 H, J_(4′,5′) 9.8, J_(4′,3′) 9.3 Hz, H-4′), 4.94 (dd, 1 H, J_(2′,3′) 9.6, J_(2′,1′) 7.9 Hz, H-2′), 4.89 (dd, 1 H, J_(2,3) 9.3, J_(2,1) 8.0 Hz, H-2), 4.83 (d, 1 H, J 12.3 Hz, PhCH). 4.56 (d, 1 H, J 12.3 Hz, PhCH), 4.51 (dd, 1 H, J_(6a,6b) 12.0, J _(6a,5) 2.0 Hz, H-6a), 4.49 (d, 1 H, J_(1,2) 8.0 Hz, H-1), 4.48 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.33 (dd, 1 H, J_(6a′,6b′) 12.5, J_(6a′,5′) 4.5 Hz, H-6a′), 4.08 (dd, 1 H, J_(6b,6a) 12.0, J_(6b,5) 5.0 Hz, H-6b), 4.01 (dd, 1 H, J_(6b′,6a′) 12.5, J_(6b′,5′) 2.3 Hz, H-6b′), 3.77 (dd, 1 H, J_(4,5) 9.6, J_(4,3) 9.3 Hz, H-4), 3.63 (ddd, 1 H, J_(5′,4′) 9.8, J_(5′,6b′) 4.5, J_(5′,6b′) 2.3 Hz, H-S′), 3.54 (ddd, 1 H, J_(5,4) 9.6, J_(5,6b) 5.0, J_(5,6a) 2.0 Hz, H-5), 2.12, 2.05, 2.00, 1.98, 1.97, 1.95 (s, 21 H, 7×OAc).

[0460] Benzyl β-cellobioside (22)

[0461] 21 (6.33 g, 8.71 mmol) was suspended in anhydrous MeOH under nitrogen when a catalytic amount of sodium methoxide was added until a basic pH was obtained. After 24 h, the reaction mixture was neutralized with acidic Amberlyte® resin. Removal of the solvent under reduced pressure yielded 22 (3.91, g) quantitatively as a white solid. ¹H NMR (D₂O, 400 MHz) selected data only: δ 7.35-7.50 (m, 5 H, Ar), 4.90 (d, 1H, J 11.6 Hz, PhCH), 4.75 (d, 1 H, J 11.6 Hz, PhCH), 4.56 (d, 1 H, J_(1,2) 8.0 Hz, H-1), 4.47 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 3.96 (dd, 1 H, J_(6a,6b) 12.1, J_(6a,5) 2.0 Hz, H-6a), 3.88 (dd, 1 H, J_(6a′,6b′) 12.6, J_(6′,5′) 2.2 Hz, H-6a′), 3.79 (dd, 1 H, J_(6b,6a) 12.1, J_(6b,5) 5.0 Hz H-6b), 3.70 (dd, 1 H, J^(6b′,6a′) 12.6, J_(6′,5′) 5.6 Hz, H-6b′).

[0462] Benzyl 2,2′,3,3′,6-penta-O-acetyl-4′,6′-O-p-methoxybenzylidene-β-cellobioside (23)

[0463] To a suspension of 22 (3.64 g, 8.42 mmol) in DMF (100 mL) was added p-anisaldehyde dimethyl acetal (1.72 mL, 10.10 mmol) followed by a catalytic amount of toluenesulphonic acid (0.03 g, 0.17 mmol). The reaction mixture was then stirred under reduced pressure (20 mm Hg) for 10 d at 60° C. After this time, solid NaHCO₃ was added to neutralize the reaction and the solvent was evaporated in vacuo. To the resulting residue was added pyridine (30 mL) and acetic anhydride (15 mL) and the mixture was stirred overnight. The volume of pyridine and acetic anhydride was then decreased by evaporation under reduced pressure and the resulting syrup was taken up in 10% v/v HCl and extracted with CH₂Cl₂ (3×80 mL). The combined organic extracts were washed with 10% v/v HCl (2×50 mL), aq. NaHCO₃ (50 mL) and water (50 mL), dried over MgSO₄ and the solvent was evaporated in vacuo. The residue was crystallized from EtOAc/Hexanes to yield 23 (3.72 g, 58%) as a white solid. ¹H NMR (CDCl₃, 400 MHz): δ 7.20-7.35 (m, 7 H. Ar), 6.80-6.90 (m, 2 H, Ar), 5.40 (s, 1 H, MeOPhCH), 5.22 (dd, 1 H, J_(3,2) 9.4, J_(3,4) 9.3 Hz, H-3), 5.11 (dd, 1 H, J_(3′,4′) 9.3, J_(3′,2′) 9.2 Hz, H-3′), 4.94 (dd, 1 H, J_(2,3) 7.9 Hz, H-2), 4.88 (dd, 1 H, J_(2′,3′) 9.2, J_(2′,1′) 7.8 Hz, H-2′), 4.84 (d, 1 H, J 12.3 Hz, PhCH), 4.57 (d, 1 H, J_(1,2) 7.9 Hz, H-1), 4.56 (d, 1 H, J 12.3 Hz, PhCH), 4.50 (dd, 1 H, J_(6a,6b) 11.9, J_(6a,5) 1.9 Hz, H-6a), 4.49 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 4.31 (dd, 1 H, J_(4′,3′) 9.3, J_(4′,5′) 4.9 Hz, H-4′), 4.07 (dd, 1 H, J_(6b,6a) 11.9, J_(6b,6a) 4.7 Hz, H-6b), 3.75-3.90 (m, 4 H, H-4, OCH₃), 3.66 (dd, 1 H, J_(6a′,6b′) 10.2, J_(6a′,5′) 9.6 Hz, H-6a′), 3.64 (dd, 1 H, J_(6b′,6a′) 10.2, J_(6b′,5′) 9.3 Hz, H-6b′), 3.53 (ddd, 1 H, J_(5,4) 9.8, J_(5,6b) 4.7, J_(5,6a) 1.9 Hz, H-5), 3.43 (ddd, 1 H, J_(5′,6a′) 9.6, J_(5′,6b′) 9.3, J_(5′,4′)4.9 Hz, H-5′), 2.12, 2.03, 2.00, 1.99, 1.97 (s, 15 H, 5×OAc).

[0464] Benzyl 2,2′,3,3′,6-penta-O-acetyl-6′-O-p-methoxybenzyl-β-cellobioside (24)

[0465] 23 (1.17 g, 1.54 mmol) was dissolved in anhydrous DMF (12 mL) when NaCNBH₃ (0.49 g, 7.72 mmol) was added. A solution of TFA (1.20 mL, 15.43 mmol) in anhydrous DMF (8 mL) was then added dropwise to the reaction mixture and the solution was allowed to stir at room temperature overnight. The reaction mixture was then filtered through Celite® and washed with CH₂Cl₂. The filtrate was added to aq NaHCO₃ (100 mL) and extracted with additional portions of CH₂Cl₂ (3×75 mL). The combined organic extracts were then washed with aq NaHCO₃ (100 mL), water (2×100 mL) and brine (100 mL), dried over MgSO₄ and the solvent was removed under reduced pressure. Chromatography over silica gel (PE:EtOAc, 1:1) afforded 24 (0.85 g, 72%) as a white solid. ¹H NMR (CDCl₃, 400 MHz): δ 7.15-7.35 (m, 7 H, Ar), 6.80-6.90 (m, 2 H, Ar), 5.09 (dd, 1 H, J_(3,2) 9.3, J_(3,4) 9.2 Hz, H-3), 4.95 (dd, 1 H, J_(3′,2′) 9.4, J_(3′,4′) 9.3 Hz, H-3′), 4.93 (dd, 1 H, J_(2,3) 9.3, J_(2,1) 7.9 Hz, H-2), 4.82 (d, 1 H, J 12.3 Hz, PhCH), 4.80 (dd, 1 H, J_(2′,3′) 9.4, J_(2′,1′) 7.9 Hz, H-2′), 4.55 (d, 1 H, J 12.3 Hz, PhCH), 4.50 (dd, 1 H, J_(6a,6b) 12.0, J_(6a,5) 2.0 Hz, H-6a), 4.47 (d, 1 H, J 11.2 Hz, MeOPhCH), 4.46 (d, 1 H, J_(1,2) 7.9 Hz, H-1), 4.44 (d, 1 H, J_(1′,2′) 7.9 Hz, H-1′), 4.41 (d, 1 H, J 11.2 Hz, MeOPhCH), 4.06 (dd, 1 H, J_(6b,6a) 12.0, J_(6b,5) 5.0 Hz, H-6b), 3.67-3.76 (m, 3 H, H-4, H-4′, H-6a′), 3.64 (dd, 1 H, J_(6b′,6a′) 9.9, J_(6b′,5′) 4.8 Hz, H-6b′), 3.52 (ddd, 1 H, J_(5,4) 9.8, J_(5,6b) 5.0, J_(5,6a) 2.0 Hz, H-5), 3.39-3.45 (m, 1 H, H-5′), 2.10, 2.03, 2.00, 1.97, 1.94 (s, 15 H, 5×OAc).

[0466] Benzyl 2,2′,3,3′,6-penta-O-acetyl-4′-deoxy-4′-fluoro-β-lactoside (25)

[0467] A solution of 24 (0.11 g, 0.15 mmol) in anhydrous CH₂Cl₂ (5 mL) under an atmosphere of argon was cooled to −20° C. before trilic anhydride (66.4 μL, 0.40 mmol) was added dropwise to the solution. The reaction mixture was stirred at room temperature for 1 h and was then diluted with 10% v/v HCl (20 mL). The mixture was extracted with CH₂Cl₂ (3×20 mL) and the combined organic layers were washed with an additional portion of 10% v/v HCl (20 mL), water (2×20 mL) and brine. After drying over MgSO₄, the solvent was evaporated under reduced pressure. The resulting residue was then dissolved in anhydrous CH₂Cl₂ and the solution was cooled to −10° C. prior to the addition of tris(dimethylamino)sulfur (trimethylsilyl)difluoride (0.12 g, 0.44 mmol). The reaction was then refluxed for 0.5 h after which time water (20 mL) was added and the reaction was extracted with CH₂Cl₂ (3×20 mL). The combined organic extracts were washed with water (2×20 mL), dried over MgSO₄ and the solvent was removed in vacua. Chromatography over silica gel (PE:EtOAc, 2:3) yielded 25 (40.3 mg, 43%) as a white solid. ¹H NMR (CDCl₃, 500 MHz): δ 7.25-7.35 (m, 5 H, Ar), 5.15 (dd, 1 H, J_(2′,3′) 10.3, J_(2′,1′) 8.0 Hz, H-2′), 5.12 (dd, 1 H, J_(3,2) 9.2, J_(3,4) 9.2 Hz, H-3), 4.96 (dd, 1 H, J_(2,s) 9.2, J_(2,1) 7.8 Hz, H-2), 4.89 (ddd, 1 H, J_(3′,F) 27.6, J_(3′,2′) 10.4, J_(3′,4′) 2.7 Hz, H-3′), 4.84 (d, 1 H, J 12.1 Hz, PhCH), 4.80 (dd, 1 H, J_(4′,F) 50.3, J_(4′,3′) 2.7 Hz, H4′), 4.57 (d, 1 H, J12.3 Hz, PhCH), 4.52 (d, 1H, J_(1′,2′) 7.4 Hz, H-1′), 4.51 (dd, 1 H, J_(6a,6b) 11.9, J_(6a,5) 2.2 Hz, H-6a), 4.49 (d, 1 H, J_(1,2) 7.8 Hz, H-1), 4.07 (dd, 1 H, J_(6b,6a) 11.9, J_(6b,5) 5.2 Hz, H-6b), 3.87 (ddd, 1 H, J_(6a′,6b′) 11.5, J_(6a′,5′) 7.5, J_(6a′,F) 1.0 Hz, H-6a′), 3.85 (dd, 1 H, J_(4,3) 9.2, J_(4,5) 9.3 Hz, H4), 3.72 (dd, 1 H, J_(6b′,6a′) 11.5, J_(6b′,5′) 4.9 Hz, H-6b′), 3.61 (ddd, 1 H, J_(5′,F) 26.4, J_(5,6a′)7.5, J_(5′,6b′) 4.9 Hz, H-5′),. 3.55-3.59 (m, 1 H, H-5), 2.11, 2.06, 2.04, 2.03, 1.98 (s, 15 H, 5×OAc). ¹⁹F NMR (CDCl₃, 188 MHz): δ-140.0 (ddd, J_(F,4′) 50.3, J_(F,3′) 27.6, J_(F,5′) 26.4 Hz).

[0468] Anal. Calcd. for C29H₃₇FO: C, 54.04; H, 5.79. Found: C, 54.32; H,5.78.

[0469] Benzyl 4′-deoxy-4′-fluoro-β-lactoside (26)

[0470] A solution of 25 (0.09 g, 0.14 mmol) in anhydrous MeOH (5 mL) under argon was made basic through the addition of a catalytic amount of sodium methoxide. The reaction mixture was stirred at room temperature overnight before it was neutralized with acidic Amberlyte® resin. Removal of the resin by filtration followed by evaporation of the solvent in vacuo gave a quantitative yield of 26 (60 mg) as a white solid. ¹H NMR (D₂O, 400 MHz) selected data only: δ 7.35-7.55 (m, 5 H, Ar), 4.91 (d, 1 H, J 11.6 Hz, PhCH), 4.54 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 4.51 (d, 1 H, J_(1,2) 6.0 Hz, H-1), 3.98 (dd, 1 H, J_(6a,6b) 12.3, J_(6a,5) 1.9 Hz, H-6a), 3.33 (dd, 1 H, J_(4,3) 8.6, J_(4,5) 8.4 Hz, H4). ¹⁹F NMR (D₂O, 188 MHz): δ-141.2 (ddd, J_(F,4′) 51.0, J_(F,3′) 30.0, J_(F,5′) 30.0 Hz).

[0471] Anal. Calcd. for C₁₉H₂₇FO₁₀: C, 52.53; H, 6.26. Found: C, 52.33; H, 6.31.

[0472] Benzyl 2,2′,3,3′,6-penta-O-acetyl-4′-deoxy-4′-iodo-6′-O-p-methoxybenzyl-β-lactoside (27)

[0473] To a stirred solution of 24 (1.22 g, 1.60 mmol) in anhydrous CH₂Cl₂ (20 mL) under argon at −20° C. was added pyridine (1.1 mL, 13.47 mmol) followed by triflic anhydride (0.73 mL, 4.33 mmol). After 5 min, the reaction mixture was allowed to warm to room temperature and then was stirred at this temperature for an additional hour. After dilution with 10% v/v HCl (65 mL), the reaction was then extracted with CH₂Cl₂ (3×65 mL). The combined organic extracts were washed with 10% v/v HCl (65 mL), water (65 mL) and brine (65 mL), dried over MgSO₄ and the solvent was evaporated under reduced pressure. The residue was dissolved in anhydrous DMF (20 mL), Nal (1.20 g, 8.02 mmol) was added and the reaction mixture was stirred at room temperature overnight. After diluting with water (75 mL) and extracting with CH₂Cl₂ (3×75 mL), the combined organic layers were then washed with water (4×75 mL) and brine (75 mL), dried over MgSO₄ and the solvent was evaporated in vacuo. The residue was chromatographed over silica gel (PE:EtOAc, 3:2) and the desired fractions were pooled and recrystallized from EtOAc/Hex to yield 27 (0.54 g, 38%) as a white solid. ¹H NMR (CDCl₃, 400 MHz): δ 7.20-7.35 (m, 7 H, Ar), 6.85-6.90 (m, 2 H, Ar), 5.15 (dd, 1 H, J_(2′,3′) 9.9, J_(2′,1′) 7.8 Hz, H-2′), 5.10 (dd, 1 H, J_(3,2) 9.5, J_(3,4) 9.3 Hz, H-3), 4.95 (dd, 1 H, J_(2,3) 9.5, J_(2,1) 7.9 Hz, H-2), 4.83 (d, 1 H, J 12.3 Hz, PhCH), 4.64 (dd, 1 H, J_(4′,3′) 4.2, J_(4′,5′) 1.1 Hz, H-4′), 4.56 (d, 1 H, J 12.3 Hz, PhCH), 4.47 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 4.43-4.49 (m, 2 H, MeOPhCH₂), 4.43 (d, 1 H, J_(1,2) 7.9 Hz, H-1), 4.43 (dd, 1 H, J_(6a,6b) 11.9, J_(6a,5) 2.0 Hz, H-6a), 4.25 (dd, 1 H, J_(3′,2′) 9.9, J_(3′,4′) 4.2 Hz, H-3′), 4.05 (dd, 1 H, J_(6b,6a) 11.9, J _(6b,5) 5.0 Hz, H-6b), 3.72-3.80 (m, 4 H, H-4, OCH₃), 3.62 (dd, 1 H, J_(6a′,6b′) 9.4, J _(6a′,5′) 5.5 Hz, H-6a′), 3.53 (ddd, 1 H, J_(5,4) 9.9, J_(5,6b) 5.0, J_(5,6a) 2.0 Hz, H-5), 3.45 (dd, 1 H, J_(6b′,6a′) 9.4, J_(6b′,5′) 7.0 Hz, H-6b′), 2.91 (ddd, 1 H, J_(5′,6b′) 7.0, J_(5′,6a′) 5.5, J_(5′,4′) 1.1 Hz, H-5′), 2.09, 2.05, 2.01, 1.98, 1.97 (s, 15 H, 5×OAc).

[0474] Benzyl 2,2′,3,3′,6-penta-O-acetyl-4′-deoxy-6′-O-p-methoxybenzyl-,β-lactoside (28)

[0475] 27 (0.50 g, 0.57 mmol) was dissolved in anhydrous benzene (15 mL), then tributyltin hydride (0.83 g, 2.87 mmol) and a catalytic amount of AIBN were added and the reaction mixture was refluxed under an atmosphere of argon. After 7 h, hexane (60 mL) was added and the reaction mixture was extracted with acetonitrile (80 mL). The acetonitrile layers were washed with two additional portions of hexane (60 mL) before the solvent was evaporated under reduced pressure. Chromatography over silica gel (PE:EtOAc, 2:1 to 3:2) yielded 28 (0.36 g, 84%) as a colourless gum. ¹H NMR (CDCl₃, 400 MHz): δ 7.15-7.35 (m, 7 H, Ar), 6.84-6.89 (m, 2 H, Ar), 5.11 (dd, 1 H, J_(3,2) 9.4, J_(3,4) 9.2 Hz, H-3), 4.94 (dd, 1 H, J_(2,3) 9.4, J_(2,1) 7.9 Hz, H-2), 4.89 (ddd, 1 H, J_(3′,4′ax) 11.5, J_(3′,2′) 9.7, J_(3′,4′eq) 5.4 Hz, H-3′), 4.82 (d, 1 H, J 12.3 Hz, PhCH), 4.76 (dd, 1 H, J_(2′,3′) 9.7, J_(2′,1′) 7.8 Hz, H-2′), 4.55 (d, 1 H, J 12.3 Hz, PhCH), 4.49 (dd, 1 H, J_(6a,6b) 12.0, J_(6a,5) 2.0 Hz, H-6a), 4.47 (d, 1 H, J_(1,2) 7.9 Hz, H-1), 4.41 (s, 2 H, MeOPhCH₂), 4.35 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 4.10 (dd, 1 H, J_(6b,6a) 12.0, J_(6b,5) 4.9 Hz, H-6b), 3.73-3.80 (m, 4 H, H-4, OCH₃), 3.51-3.64 (m, 2 H, H-5, H-5′), 3.51 (dd, 1 H, J_(6a′,6b′) 9.8, J_(6a′,5′) 5.1 Hz, H-6a′), 3.40 (dd, 1 H, J_(6b′,6a′) 9.8, J_(6b′,5′) 5.0 Hz, H-6b′), 2.09,2.01, 1.97, 1.95 (s, 15 H, 5×OAc), 1.47-1.63 (m, 2 H, H-4′_(ax), H-4′_(eq)).

[0476] Benzyl 2,2′,3,3′,6-penta-O-acetyl-4′-deoxy-β-lactoside (29)

[0477] Ceric ammonium nitrate (0.55 g, 1.00 mmol) was added to a solution of 28 (0.34 g, 0.46 mmol) in 9:1 acetonitrile/water (4 mL) and the reaction mixture was stirred at room temperature for 6 h before being added to aq. NaHCO₃ (15 mL) and extracted with CH₂Cl₂ (3×15 mL). The combined organic extracts were washed with aq. NaHCO₃ (15 mL), water (15 mL) and brine (15 mL), dried over MgSO₄ and the solvent was evaporated under reduced pressure. The resulting residue was crystallized from EtOAc/Hex to yield 29 (232 mg, 81%) as a white needle-like solid. ¹H NMR (CDCl₃, 400 MHz): δ 7.20-7.35 (m, 5 H, Ar), 5.14 (dd, 1 H, J_(3,2) 92, J_(3,4) 9.1 Hz, H-3), 4.94 (dd, 1H, J_(2,3) 9.2, J_(2,1) 7.8 Hz, H-2), 4.88-4.96 (m, 1 H, H-3′), 4.83 (d, 1 H, J 12.3 Hz, PhCH), 4.78 (dd, 1 H, J_(2′,3′) 9.4, J_(2′,1′) 7.7 Hz, H-2′), 4.57 (d, 1 H, J 12.3 Hz, PhCH), 4.51 (dd, 1 H, J_(6a,6b) 11.8, J_(6a,5) 2.1 Hz, H-6a), 4.49 (d, 1 H, J_(1,2) 7.8 Hz, H -1), 4.46 (d, 1 H, J_(1′,2′) 7.7 Hz, H-1′), 4.08 (dd, 1 H, J_(6b,6a) 11.8, J_(6b,5) 5.3 Hz, H-6b), 3.82 (dd, 1 H, J_(4,5) 9.5, J_(4,3) 9.1 Hz, H-4), 3.51-3.64 (m, 4 H, H-5, H-5′, H-6a′, H-6b′), 2.11, 2.04, 2.03, 1.98, 1.97 (s, 15 H, 5×OAc), 1.46-1.60 (m, 2 H, H-4′_(ax), H-4′_(eq)).

[0478] Anal. Calcd. for C₂₉H₃₈O₁₅: C, 55.59; H, 6.11. Found: C, 55.91; H, 6.16.

[0479] Benzyl 4′-deoxy-β-lactoside (30)

[0480] A solution of 29 (0.21 g, 0.33 mmol) in anhydrous MeOH (10 mL) under argon was made basic through the addition of a catalytic amount of sodium methoxide. The reaction mixture was stirred at room temperature overnight before it was neutralized with acidic Amberlyte® resin. Removal of the resin by filtration followed by evaporation of the solvent in vacuo gave a quantitative yield of 30 (147 mg) as a white solid. m.p 169-171° C. ¹H NMR (CD₃OD, 400 MHz) selected data only: δ 7.22-7.45 (m, 5 H, Ar), 4.91 (d, 1H, J 11.8 Hz, PhCH), 4.66 (d, 1 H, J 11.8 Hz, PhCH), 4.39 (d, 1 H, J_(1,2) 7.8 Hz, H-1), 4.34 (d, 1 H, J_(1′,2′) 7.8 Hz, H-1′), 3.93 (dd, 1 H, J_(6a,6b) 12.1, J_(6a,5) 2.4 Hz, H-6a), 3.86 (dd, 1 H, J_(6b,6a) 12.1, J_(6b,5) 4.2 Hz, H-6b), 3.13 (dd, 1 H, J_(4,5) 8.7, J_(4,3) 8.1 Hz, H4), 1.89 (dd, 1 H, J_(4′eq,4′ax) 12.7, J_(4′eq,3′) 5.0 Hz, H-4′_(eq)), 1.41 (ddd, 1 H, J_(4′ax,4′eq) 12.7, J_(4′ax,3′) 11.9, J_(4′ax,5′) 11.9 Hz, H-4′_(ax)).

[0481] Anal. Calcd. for C₁₉H₂₈O₁₀: C, 54.80; H, 6.78. Found: C, 54.50; H, 6.72.

[0482] Synthesis of ¹⁸O-UDPGal:

[0483] Diphenyl (2,3,4,6-tetra-O-acetyl)-[1-¹⁸O]-α-D-galactopyranosyl Phosphate (31)

[0484] To a solution of 2,3,4,6-tetra-O-acetyl-D-galactose (0.49 g, 1.41 mmol) in anhydrous acetonitrile (2 mL) in a thick walled bomb was added 97% ¹⁸O-enriched water (0.5 mL). A few beads of Amberlyte® IR-120 acidic resin were added and the chamber was flooded with argon and sealed. The reaction mixture was then heated to 105° C. for 24 h. After this time, the solvent was removed in vacuo and the residue was chromatographed over silica gel (PE:EtOAc, 3:2 to 1:1). This 1-¹⁸O-labeled 2,3,4,6-tetra-O-acetyl-D-galactopyranose along with DMAP (025 g, 2.03 mmol) were then dissolved in anhydrous CH₂Cl₂ and stirred at room temperature for 20 min under an atmosphere of argon. Diphenyl chlorophosphate (0.54 g, 2.03 mmol) was then added to the reaction mixture and stirring was continued for 3 h, when it was then added to a 10% v/v solution of HCl (40 mL) and extracted with CH₂Cl₂ (3×40 mL). The combined organic extracts were washed with aq. NaHCO₃ (35 mL) and water (3×35 mL), dried over MgSO₄ and the solvent was evaporated under reduced pressure. Chromatography over silica gel (PE:EtOAc, 12:7 to 3:2) yielded 31 (316.1 mg, 39%) as a colourless gum. ¹HNMR(CDCl₃, 400 MHz): δ 7.15-7.45 (m, 10 H, Ar), 6.10 (dd, 1 H, J_(1,F) 6.4, J _(1,2) 3.3 Hz, H-1), 5.47 (dd, 1 H, J_(4,3) 3.1, J_(4,5) 1.1 Hz, H-4), 5.37 (dd, 1 H, J_(3,2) 10.9, J_(3,4) 3.1 Hz, H-3), 5.23 (ddd, 1 H J_(2,3) 10.9, J_(2,1) 3.3, J_(2,P) 3.0 Hz, H-2), 4.32 (ddd, 1 H, J_(5,6a) 6.6, J _(5,6b) 6.5, J_(5,4) 1.1 Hz, H-5), 4.06 (dd, 1 H, J_(6a,6b) 11.3, J_(6a,5) 6.6 Hz, H-6a), 3.91 (dd, 1 H, J_(6b,6a) 11.3, J_(6b,5) 6.5 Hz, H-6b), 2.12, 1.97, 1.90, 1.83 (s, 12 H, 4×OAc). ³¹P NMR (CDCl₃, 81 MHz, proton decoupled): δ-13.70. LR-LSIMS: calcd. for C₂₆H₂₉O₁₃P: 581. Found: 581 (C₂₆H₂₉ ¹⁶O₁₃P), 583 (C₂₆H₂₉ ¹⁶O₁₂ ¹⁸OP), ¹⁶O /¹⁸O=20/80.

[0485] α-D-Galactopyranosyl-[1-¹⁸O]-phosphate Monopyridinium Salt (32)

[0486] 31 (0.31 g, 0.54 mmol) was dissolved in 1:1 EtOAc:MeOH (6 mL) when PtO₂ (0.10 g) was added and the reaction mixture was hydrogenated at 6 atm. After 2 d, this mixture was filtered through Celite® and chromatographed over silica gel (EtOAc to EtOAc:MeOH:H₂O, 27:2:1 to 7:2:1). The desired fractions were pooled, concentrated and redissolved in THF (1 mL). To this was then added 2 M LiOH (2 mL) and the reaction mixture was allowed to stir at room temperature overnight. The reaction volume was then reduced and eluted through a Bio-Rad® AG 50W-X2, 200-400 mesh sulfonic acid cation exchange column (pyridinium form). The desired fractions were pooled and lyophilized to yield 32 (126 mg, 69%) as a white fluffy solid ¹H NMR (D₂O, 300 MHz): δ 7.90-8.70 (m, 5 H, pyridine), 5.40 (dd, 1 H, J_(1,P) 7.0, J_(3,2) 3.5 Hz, H-1), 4.00 (dd, 1 H, J_(5,6a) 6.3, J_(5,6b) 6.3 Hz, H-5), 3.88 (d, 1 H, J_(4,3) 2.9 Hz, H-4), 3.77 (dd, 1 H, J_(3,2) 10.3, J_(3,4) 2.9 Hz, H-3), 3.68 (ddd, 1 H, J_(2,3) 10.3, J_(2,1) 3.5, J_(2,P) 3.0 Hz, H-2), 3.53-3.63 (m, 2 H, H-6a, H-6b). ³¹P NMR (D₂O, 121 MHz, proton decoupled): δ 0.09. LR-LSIMS: calcd for C₆H₁₂O₉P-: 259. Found: 259 (C₆H₁₂ ¹⁶O₉P⁻), 261 (C₆H₁₂ ¹⁶O₈ ¹⁸OP⁻), ¹⁶O/¹⁸O=17/83.

[0487] Uridine 5′-diphospho-[1″-¹⁸O-α-D-galactopyranose, Diammonium Salt (33)

[0488] To a solution of 32 (0.08 g, 0.24 mmol) in water (1.5 mL) was added tri-n-octylamine (0.10 mL, 0.24 mmol) and the mixture was lyophilized. The resulting residue along with UMP-morpholidate (0.18 g, 0.26 mmol) was dried over P₂O₅ overnight. The two reagents were then dissolved in anhydrous pyridine (2.5 mL) and the reaction mixture was stirred at room temperature in the presence of 4 Å molecular sieves under an argon atmosphere. An aliquot of the reaction mixture was transferred into an NMR tube containing a capillary of DMSO-d6 so that the reaction progress can be monitored by ³¹P NMR. After 11 d, the mixture was filtered and the filtrate was added to 50 mM NH₄HCO₃. The tri-n-octylamine was extracted with Et₂O (3×15 mL) and the aqueous phase was lyophilized to yield the crude product. Purification was afforded by anion exchange chromatography on a DEAE Sephacel column (26 mm×12.5 cm, 50-500 mM NH₄HCO₃, 1.5 mL/min) followed by size exclusion chromatography on a Bio-Gel P2, extra fine column (16 mm×55 cm, 50 mM NH₄HCO₃, 0.15 mL/min) using a Beckman Biosepra ProSys Workstation. The desired fractions were pooled and lyophilized to yield 33 (25 mg, 18%) as a white powder. ¹H NMR (D₂O, 300 MHz): δ 7.83 (d, 1 H, J_(6,5) 8.2 Hz, H-6), 5.30-5.40 (m, 2 H, H-5, H-1′), 5.53 (dd, 1 H, J_(1″,P) 7.2, J_(1″,2″) 3.6 Hz, H-1″), 4.23-4.28 (m, 2 H, H-2′, H-3′), 4.07-4.20 (m, 3 H, H4′, H-5a′, H-5b′), 4.06 (dd, 1 H, J_(5″,6a″) 6.2, J_(5″, 6b″) 6.2 Hz, H-5″), 3.92 (d, 1 H, J_(4″,3″) 3.0 Hz, H-4″), 3.80 (dd, 1 H, J_(3″,2″) 10.2, J_(3″,4″) 3.0 Hz, H-3″), 3.68 (ddd, 1 H, J_(2″,3″) 10.2, J_(2″,1″) 3.6, J_(2″,P) 3.0 Hz, H-2″), 3.55-3.65 (m, 2 H, H-6a″, H-6b″). ³¹P NMR (D₂O, 121 MHz, proton decoupled): δ-9.95 (d, 1P, J_(Pβ,Pα) 20.1 Hz, P^(β)), -11.51 (d, 1P, J_(Pα,Pβ) 20.7 Hz, P^(α)). HR-LSIMS: calcd. for C₁₅H₂₃N₂ ¹⁶O₁₆ ¹⁸OP₂ ⁻: 567.0513. Found 567.0515. LR-LSIMS: ¹⁶O/¹⁸O=15/85.

[0489] Anal. Calcd. for C₁₅H₂₂N₂ ¹⁶O₁₆ ¹⁸OP₂ ²⁻.2NH₄ ⁺: C, 29.86; H, 5.18; N, 9.29. Found: C, 30.21; H, 5.16; N, 8.97.

[0490] All publications mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described methods and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in chemistry, biology or related fields are intended to be within the scope of the following claims. TABLE 1 Kinetic parameters of wild-type LgtC and its various mutants for its substrates UDP-Gal and lactose. UDP-Gal² Lactose³ k_(cat) K_(m) k_(cat) K_(m) k_(cat)/K_(m) LgtC¹ (s)⁻¹ (μM) k_(cat)/K_(m (μM) ⁻¹s⁻¹) (s)⁻¹ (mM) (mM⁻¹s⁻¹) WT 14.2 18 0.81 24.0 20 1.20 C128/174S 11.4 12 0.97 19.2 13 1.48 D103E 0.004 218 0.00002 0.003 34 0.00009 D103N 0.006 187 0.00003 0.006 58 0.00010 Y186F 25.6 15 1.67 31.6 16 1.92 Q189A 0.4 25 0.017 1.0 136 0.0074

[0491] TABLE 2 Data collection and refinement statistics¹ Data collection 4-deoxy- Peak Inflection Remote1 Remote2 lactose Resolution (Å) 20-2.0 20-2.0 20-2.0 20-2.0 20-2.0 Wavelength 0.97949 0.97996 0.92526 1.06883 1.5418 (Å) Unique 18498 18492 18400 18516 18851 reflections Completeness 99.0 99.0 98.9 97.2 98.3 (%) (97.7) (97.7) (97.8) (83.9) (90.2) I/I(σ) 19.8 19.9 19.1 19.7 20.7  (6.1)  (6.1)  (5.9)  (5.1) (8.03) Rmerge (%) 4.4 4.4 4.7 4.2 6.2 (11.4) (11.4) (12.3)  (9.2) (15.2)

[0492] Refinement statistics and model stereochemistry LgtC/Mn/donor LgtC/Mn/donor/acceptor Resolution (Å) 20-2.0 20-2.0 Unique reflections 18038 18225 Rcryst/Rfree (%) 19.9/22.74 19.3/22.76 RMSD bonds (Å) 0.007 0.007 RMSD angles (°) 1.31 1.33 Average B-factor (Å²) Protein 13.5 16.3 UDP 2-deoxy-2-fluoro- 11.6 15.4 galactose 4-deoxylactose 19.8 Mn 5.3 11.3 Water 21.1 23.6 Ramachandran plot Residues in most favored 92.2 91.0 regions (%) Additionally allowed 7.0 8.6 regions (%) Generously allowed regions 0.4 0.4 (%) Disallowed regions (%) 0.4 0

[0493] TABLE 3 Atomic Interactions of a Retaining Glycosyltransferase with a Sugar Nucleotide Donor and/or Acceptor Molecules Atomic Contact on Sugar Nucleotide No. of Atomic Donor or Acceptor Binding Site Interaction Molecules Atomic Contact on Enzyme Property 1 Uracil O2 Main chain nitrogen of Asp 8 HB 2 Uracil N3 OD1 of Asp 8 HB 3 Uracil carbonyl 04 ND2 group of Asn 10 HB 4 Ribose ring 02 Carbonyl oxygen of Ala 6 5 Ribose O3 Main chain amide of Ile 104 6 Phosphate 02A Lys 250 (NZ) HB 7 Phosphate 02B Gly 247 (N) and His 78 (NE2) HB 8 Sugar donor ring O3 Asp 103 and Arg 86 HB 9 Sugar donor ring 04′ Carboxylate of Asp 188 HB 10 Sugar donor ring 06′ Carboxylate of Asp 188 HB 11 Mn²⁺ His 244, Asp 103, Asp 105 12 Lactose 06 Asp 130 (OD2) and Gln 189 (NE2) HB 13 Lactose 06 Side chain atoms of Val 76, His 78, Tyr VdW 186, Cys 246, and Gly 247 14 Reducing end glucose Phe 132 HP moiety of lactose 15 Pro 211 and Pro 248 VdW 16 Reducing end glucose Thr 212 hydroxyl, main chain nitrogen HB moiety of lactose 03′ 17 Cys 246 HB

[0494] REMARK coordinates from minimization refinement REMARK refinement resolution: 20.0-2.0 A REMARK starting r = .2046 free_r = .2331 REMARK final r = .2033 free_r = .2321 REMARK rmsd bonds = .005248 rmsd angles = 1.22351 REMARK wa = .890542 REMARK target = mlf cycles = 1 steps = 100 REMARK sg = P2 (1) 2 (1) 2 (1) a = 39.79 b = 76.05 c = 86.84 alpha = 90 beta = 90 gamma = 90 REMARK parameter file 1: CNS_TOPPAR:protein_rep.param REMARK parameter file 2: ../rnd4/upg.par REMARK parameter file 3: CNS_TOPPAR:ion.param REMARK parameter file 4: CNS_TOPPAR:water_rep.param REMARK parameter file 5: ../rnd6/acy.par REMARK molecular structure file: generate7_2.mtf REMARK input coordinates: generate7_2.pdb REMARK reflection file = ../lgtC.cv REMARK ncs = none REMARK B-correction resolution: 6.0-2.0 REMARK initial B-factor correction applied to fobs: REMARK B11 = 1.111 B22 = 2.062 B33 = −3.173 REMARK B12 = .000 B13 = .000 B23 = .000 REMARK B-factor correction applied to coordinate array B: .174 REMARK bulk solvent: density level = .335425 e/A{circumflex over ( )}3, B-factor = 42.4467 A{circumflex over ( )}2 REMARK reflections with |Fobs|/sigma_F < 0.0 rejected REMARK reflections with |Fobs| > 10000 * rms (Fobs) rejected REMARK theoretical total number of refl. in resol. range: 18411 (100.0%) REMARK number of unobserved reflections (no entry or |F|= 0): 373 (2.0%) REMARK number of reflections rejected: 0 (>.0%) REMARK total number of reflections used: 18038 (>98.0%) REMARK number of reflections in working set: 17161 (>93.2%) REMARK number of reflections in test set: 877 (>4.8%) CRYST1 39.790 76.050 86.840 90.00 90.00 90.00 P 21 21 21 REMARK FILENAME = “minimize7_3.pdb” REMARK DATE: 29-May-00 21:53:49 created by user: karina REMARK VERSION: 1.0 ATOM 1 CB MSE 1 47.916 46.223 65.035 1.00 15.18 DIC ATOM 2 CG MSE 1 47.459 47.194 63.956 1.00 18.95 DIC ATOM 3 SE MSE 1 46.533 48.765 64.672 1.00 23.16 DIC ATOM 4 CE MSE 1 48.073 49.691 65.392 1.00 19.79 DIC ATOM 5 C MSE 1 47.671 44.106 63.711 1.00 10.02 DIC ATOM 6 O MSE 1 47.762 44.051 62.487 1.00 9.02 DIC ATOM 7 N MSE 1 49.817 45.335 63.713 1.00 9.31 DIC ATOM 8 CA MSE 1 48.632 44.961 64.526 1.00 10.07 DIC ATOM 9 N ASP 2 46.762 43.426 64.398 1.00 8.25 DIC ATOM 10 CA ASP 2 45.786 42.580 63.729 1.00 8.29 DIC ATOM 11 CB ASP 2 45.742 41.193 64.376 1.00 8.73 DIC ATOM 12 CG ASP 2 47.016 40.405 64.139 1.00 11.00 DIC ATOM 13 OD1 ASP 2 47.966 40.549 64.934 1.00 9.98 DIC ATOM 14 OD2 ASP 2 47.073 39.655 63.139 1.00 12.73 DIC ATOM 15 C ASP 2 44.413 43.224 63.763 1.00 6.99 DIC ATOM 16 O ASP 2 43.839 43.440 64.831 1.00 5.46 DIC ATOM 17 N ILE 3 43.906 43.535 62.573 1.00 7.26 DIC ATOM 18 CA ILE 3 42.604 44.172 62.399 1.00 5.51 DIC ATOM 19 CB ILE 3 42.680 45.315 61.356 1.00 6.61 DIC ATOM 20 CG2 ILE 3 41.276 45.917 61.119 1.00 3.06 DIC ATOM 21 CG1 ILE 3 43.692 46.372 61.806 1.00 4.70 DIC ATOM 22 CD ILE 3 43.312 47.108 63.082 1.00 7.67 DIC ATOM 23 C ILE 3 41.585 43.166 61.893 1.00 6.14 DIC ATOM 24 O ILE 3 41.881 42.379 60.990 1.00 6.52 DIC ATOM 25 N VAL 4 40.388 43.205 62.472 1.00 5.89 DIC ATOM 26 CA VAL 4 39.302 42.322 62.072 1.00 4.89 DIC ATOM 27 CB VAL 4 38.791 41.468 63.248 1.00 6.30 DIC ATOM 28 CG1 VAL 4 37.584 40.638 62.795 1.00 8.75 DIC ATOM 29 CG2 VAL 4 39.904 40.558 63.753 1.00 5.68 DIC ATOM 30 C VAL 4 38.115 43.110 61.519 1.00 5.54 DIC ATOM 31 O VAL 4 37.688 44.111 62.097 1.00 4.90 DIC ATOM 32 N PHE 5 37.603 42.655 60.382 1.00 5.50 DIC ATOM 33 CA PHE 5 36.449 43.260 59.728 1.00 5.20 DIC ATOM 34 CB PHE 5 36.832 43.859 58.364 1.00 5.40 DIC ATOM 35 CG PHE 5 37.439 45.234 58.430 1.00 4.45 DIC ATOM 36 CD1 PHE 5 36.693 46.323 58.876 1.00 4.41 DIC ATOM 37 CD2 PHE 5 38.732 45.453 57.969 1.00 5.91 DIC ATOM 38 CE1 PHE 5 37.228 47.619 58.851 1.00 6.66 DIC ATOM 39 CE2 PHE 5 39.276 46.743 57.940 1.00 7.08 DIC ATOM 40 CZ PHE 5 38.516 47.828 58.381 1.00 6.75 DIC ATOM 41 C PHE 5 35.501 42.090 59.479 1.00 6.22 DIC ATOM 42 O PHE 5 35.929 40.934 59.475 1.00 6.65 DIC ATOM 43 N ALA 6 34.222 42.390 59.282 1.00 4.81 DIC ATOM 44 CA ALA 6 33.221 41.372 58.988 1.00 4.67 DIC ATOM 45 CB ALA 6 32.352 41.084 60.213 1.00 2.66 DIC ATOM 46 C ALA 6 32.366 41.944 57.872 1.00 5.29 DIC ATOM 47 O ALA 6 31.920 43.090 57.952 1.00 4.39 DIC ATOM 48 N ALA 7 32.132 41.164 56.826 1.00 5.20 DIC ATOM 49 CA ALA 7 31.314 41.669 55.736 1.00 6.73 DIC ATOM 50 CB ALA 7 32.120 42.659 54.901 1.00 8.23 DIC ATOM 51 C ALA 7 30.755 40.590 54.834 1.00 8.12 DIC ATOM 52 O ALA 7 31.340 39.515 54.695 1.00 7.34 DIC ATOM 53 N ASP 8 29.598 40.885 54.247 1.00 8.39 DIC ATOM 54 CA ASP 8 28.967 39.987 53.295 1.00 8.38 DIC ATOM 55 CB ASP 8 27.449 39.915 53.502 1.00 9.33 DIC ATOM 56 CG ASP 8 26.832 41.261 53.816 1.00 9.71 DIC ATOM 57 OD1 ASP 8 27.334 42.290 53.312 1.00 8.87 DIC ATOM 58 OD2 ASP 8 25.828 41.285 54.561 1.00 9.54 DIC ATOM 59 C ASP 8 29.294 40.608 51.941 1.00 9.19 DIC ATOM 60 O ASP 8 29.926 41.664 51.878 1.00 7.12 DIC ATOM 61 N ASP 9 28.873 39.969 50.859 1.00 9.74 DIC ATOM 62 CA ASP 9 29.180 40.485 49.532 1.00 10.05 DIC ATOM 63 CB ASP 9 28.551 39.582 48.471 1.00 10.66 DIC ATOM 64 CG ASP 9 29.132 39.817 47.098 1.00 10.96 DIC ATOM 65 OD1 ASP 9 30.353 39.613 46.927 1.00 9.95 DIC ATOM 66 OD2 ASP 9 28.370 40.210 46.192 1.00 15.56 DIC ATOM 67 C ASP 9 28.731 41.935 49.328 1.00 11.33 DIC ATOM 68 O ASP 9 29.427 42.729 48.689 1.00 11.67 DIC ATOM 69 N ASN 10 27.578 42.282 49.889 1.00 11.40 DIC ATOM 70 CA ASN 10 27.033 43.626 49.760 1.00 12.66 DIC ATOM 71 CB ASN 10 25.707 43.721 50.518 1.00 14.73 DIC ATOM 72 CG ASN 10 25.079 45.098 50.424 1.00 16.23 DIC ATOM 73 OD1 ASN 10 24.924 45.644 49.335 1.00 16.14 DIC ATOM 74 ND2 ASN 10 24.706 45.662 51.569 1.00 15.48 DIC ATOM 75 C ASN 10 27.972 44.730 50.244 1.00 12.57 DIC ATOM 76 O ASN 10 27.962 45.839 49.705 1.00 12.93 DIC ATOM 77 N TYR 11 28.782 44.432 51.254 1.00 10.65 DIC ATOM 78 CA TYR 11 29.702 45.425 51.805 1.00 10.78 DIC ATOM 79 CB TYR 11 29.632 45.399 53.336 1.00 10.58 DIC ATOM 80 CG TYR 11 28.703 46.427 53.944 1.00 11.86 DIC ATOM 81 CD1 TYR 11 27.599 46.915 53.239 1.00 11.68 DIC ATOM 82 CE1 TYR 11 26.737 47.853 53.811 1.00 12.47 DIC ATOM 83 CD2 TYR 11 28.918 46.900 55.239 1.00 11.28 DIC ATOM 84 CE2 TYR 11 28.063 47.829 55.818 1.00 13.50 DIC ATOM 85 CZ TYR 11 26.978 48.301 55.101 1.00 12.90 DIC ATOM 86 OH TYR 11 26.144 49.225 55.681 1.00 15.54 DIC ATOM 87 C TYR 11 31.155 45.267 51.369 1.00 11.16 DIC ATOM 88 O TYR 11 32.043 45.919 51.925 1.00 11.02 DIC ATOM 89 N ALA 12 31.400 44.421 50.371 1.00 10.59 DIC ATOM 90 CA ALA 12 32.760 44.183 49.892 1.00 10.32 DIC ATOM 91 CB ALA 12 32.744 43.157 48.754 1.00 11.38 DIC ATOM 92 C ALA 12 33.489 45.450 49.441 1.00 9.91 DIC ATOM 93 O ALA 12 34.660 45.647 49.766 1.00 9.42 DIC ATOM 94 N ALA 13 32.804 46.306 48.688 1.00 9.60 DIC ATOM 95 CA ALA 13 33.414 47.540 48.205 1.00 9.28 DIC ATOM 96 CB ALA 13 32.481 48.229 47.204 1.00 9.14 DIC ATOM 97 C ALA 13 33.756 48.491 49.355 1.00 8.84 DIC ATOM 98 O ALA 13 34.815 49.125 49.357 1.00 8.22 DIC ATOM 99 N TYR 14 32.865 48.582 50.336 1.00 8.07 DIC ATOM 100 CA TYR 14 33.090 49.462 51.478 1.00 8.03 DIC ATOM 101 CB TYR 14 31.803 49.606 52.291 1.00 8.61 DIC ATOM 102 CG TYR 14 30.600 49.939 51.438 1.00 10.64 DIC ATOM 103 CD1 TYR 14 30.700 50.855 50.394 1.00 11.14 DIC ATOM 104 CE1 TYR 14 29.602 51.168 49.602 1.00 13.63 DIC ATOM 105 CD2 TYR 14 29.363 49.340 51.676 1.00 11.59 DIC ATOM 106 CE2 TYR 14 28.252 49.647 50.891 1.00 14.49 DIC ATOM 107 CZ TYR 14 28.384 50.563 49.854 1.00 14.26 DIC ATOM 108 OH TYR 14 27.302 50.879 49.068 1.00 17.66 DIC ATOM 109 C TYR 14 34.222 48.934 52.356 1.00 7.50 DIC ATOM 110 O TYR 14 34.995 49.710 52.914 1.00 8.49 DIC ATOM 111 N LEU 15 34.310 47.612 52.469 1.00 7.68 DIC ATOM 112 CA LEU 15 35.363 46.965 53.247 1.00 7.83 DIC ATOM 113 CB LEU 15 35.267 45.440 53.105 1.00 7.70 DIC ATOM 114 CG LEU 15 36.519 44.619 53.441 1.00 8.87 DIC ATOM 115 CD1 LEU 15 36.881 44.790 54.913 1.00 7.99 DIC ATOM 116 CD2 LEU 15 36.265 43.146 53.117 1.00 8.32 DIC ATOM 117 C LEU 15 36.719 47.428 52.729 1.00 6.26 DIC ATOM 118 O LEU 15 37.605 47.790 53.503 1.00 5.67 DIC ATOM 119 N CYS 16 36.868 47.407 51.407 1.00 6.41 DIC ATOM 120 CA CYS 16 38.109 47.814 50.761 1.00 6.53 DIC ATOM 121 CB CYS 16 37.972 47.683 49.241 1.00 7.09 DIC ATOM 122 SG CYS 16 39.490 48.066 48.352 1.00 10.90 DIC ATOM 123 C CYS 16 38.509 49.245 51.122 1.00 6.22 DIC ATOM 124 O CYS 16 39.673 49.521 51.415 1.00 6.80 DIC ATOM 125 N VAL 17 37.545 50.156 51.101 1.00 6.94 DIC ATOM 126 CA VAL 17 37.823 51.548 51.436 1.00 7.93 DIC ATOM 127 CB VAL 17 36.583 52.436 51.173 1.00 8.98 DIC ATOM 128 CG1 VAL 17 36.840 53.854 51.651 1.00 8.40 DIC ATOM 129 CG2 VAL 17 36.260 52.436 49.679 1.00 9.77 DIC ATOM 130 C VAL 17 38.240 51.670 52.900 1.00 7.79 DIC ATOM 131 O VAL 17 39.233 52.316 53.217 1.00 7.46 DIC ATOM 132 N ALA 18 37.481 51.041 53.790 1.00 7.51 DIC ATOM 133 CA ALA 18 37.789 51.091 55.213 1.00 7.78 DIC ATOM 134 CB ALA 18 36.750 50.295 56.005 1.00 7.26 DIC ATOM 135 C ALA 18 39.188 50.530 55.471 1.00 7.32 DIC ATOM 136 O ALA 18 39.978 51.125 56.201 1.00 8.92 DIC ATOM 137 N ALA 19 39.491 49.387 54.864 1.00 6.80 DIC ATOM 138 CA ALA 19 40.796 48.761 55.046 1.00 6.34 DIC ATOM 139 CB ALA 19 40.866 47.448 54.275 1.00 7.20 DIC ATOM 140 C ALA 19 41.904 49.698 54.585 1.00 9.12 DIC ATOM 141 O ALA 19 42.917 49.854 55.267 1.00 7.42 DIC ATOM 142 N LYS 20 41.714 50.333 53.431 1.00 9.41 DIC ATOM 143 CA LYS 20 42.736 51.243 52.937 1.00 10.30 DIC ATOM 144 CB LYS 20 42.404 51.725 51.523 1.00 11.46 DIC ATOM 145 CG LYS 20 43.560 52.483 50.883 1.00 17.23 DIC ATOM 146 CD LYS 20 43.346 52.750 49.404 1.00 19.42 DIC ATOM 147 CE LYS 20 44.561 53.444 48.812 1.00 21.28 DIC ATOM 148 NZ LYS 20 44.387 53.756 47.368 1.00 22.28 DIC ATOM 149 C LYS 20 42.912 52.435 53.881 1.00 10.50 DIC ATOM 150 O LYS 20 44.017 52.950 54.027 1.00 8.75 DIC ATOM 151 N SER 21 41.836 52.872 54.533 1.00 9.94 DIC ATOM 152 CA SER 21 41.959 53.997 55.459 1.00 9.54 DIC ATOM 153 CB SER 21 40.586 54.438 55.988 1.00 10.25 DIC ATOM 154 OG SER 21 40.096 53.556 56.983 1.00 11.69 DIC ATOM 155 C SER 21 42.859 53.588 56.626 1.00 7.93 DIC ATOM 156 O SER 21 43.587 54.411 57.172 1.00 8.07 DIC ATOM 157 N VAL 22 42.807 52.314 57.006 1.00 8.61 DIC ATOM 158 CA VAL 22 43.639 51.817 58.102 1.00 7.31 DIC ATOM 159 CB VAL 22 43.225 50.397 58.540 1.00 7.87 DIC ATOM 160 CG1 VAL 22 44.163 49.901 59.630 1.00 7.62 DIC ATOM 161 CG2 VAL 22 41.792 50.404 59.043 1.00 7.19 DIC ATOM 162 C VAL 22 45.107 51.785 57.684 1.00 8.07 DIC ATOM 163 O VAL 22 45.992 52.151 58.460 1.00 8.06 DIC ATOM 164 N GLU 23 45.371 51.340 56.460 1.00 7.76 DIC ATOM 165 CA GLU 23 46.749 51.296 55.977 1.00 9.02 DIC ATOM 166 CB GLU 23 46.832 50.605 54.609 1.00 9.88 DIC ATOM 167 CG GLU 23 46.444 49.125 54.602 1.00 11.02 DIC ATOM 168 CD GLU 23 46.763 48.450 53.276 1.00 13.23 DIC ATOM 169 OE1 GLU 23 46.541 49.086 52.228 1.00 15.00 DIC ATOM 170 OE2 GLU 23 47.221 47.285 53.279 1.00 12.64 DIC ATOM 171 C GLU 23 47.309 52.714 55.858 1.00 8.76 DIC ATOM 172 O GLU 23 48.447 52.976 56.246 1.00 8.97 DIC ATOM 173 N ALA 24 46.503 53.630 55.328 1.00 7.51 DIC ATOM 174 CA ALA 24 46.939 55.011 55.152 1.00 7.86 DIC ATOM 175 CB ALA 24 45.825 55.834 54.493 1.00 8.90 DIC ATOM 176 C ALA 24 47.367 55.664 56.465 1.00 8.07 DIC ATOM 177 O ALA 24 48.332 56.436 56.499 1.00 6.11 DIC ATOM 178 N ALA 25 46.654 55.353 57.543 1.00 7.25 DIC ATOM 179 CA ALA 25 46.961 55.923 58.853 1.00 7.99 DIC ATOM 180 CB ALA 25 45.705 55.908 59.736 1.00 6.76 DIC ATOM 181 C ALA 25 48.112 55.212 59.569 1.00 8.57 DIC ATOM 182 O ALA 25 48.504 55.611 60.663 1.00 7.27 DIC ATOM 183 N HIS 26 48.646 54.157 58.960 1.00 8.84 DIC ATOM 184 CA HIS 26 49.758 53.424 59.563 1.00 9.94 DIC ATOM 185 CB HIS 26 49.258 52.138 60.227 1.00 10.38 DIC ATOM 186 CG HIS 26 48.185 52.363 61.246 1.00 12.18 DIC ATOM 187 CD2 HIS 26 48.251 52.548 62.587 1.00 12.40 DIC ATOM 188 ND1 HIS 26 46.848 52.431 60.917 1.00 12.47 DIC ATOM 189 CE1 HIS 26 46.137 52.644 62.010 1.00 13.32 DIC ATOM 190 NE2 HIS 26 46.965 52.719 63.037 1.00 11.84 DIC ATOM 191 C HIS 26 50.804 53.090 58.502 1.00 8.30 DIC ATOM 192 O HIS 26 51.035 51.923 58.179 1.00 7.59 DIC ATOM 193 N PRO 27 51.465 54.124 57.959 1.00 8.95 DIC ATOM 194 CD PRO 27 51.399 55.521 58.424 1.00 9.38 DIC ATOM 195 CA PRO 27 52.490 53.970 56.927 1.00 9.59 DIC ATOM 196 CB PRO 27 52.940 55.408 56.672 1.00 10.14 DIC ATOM 197 CG PRO 27 52.738 56.064 57.999 1.00 11.05 DIC ATOM 198 C PRO 27 53.652 53.045 57.278 1.00 10.29 DIC ATOM 199 O PRO 27 54.227 52.414 56.389 1.00 12.94 DIC ATOM 200 N ASP 28 54.000 52.949 58.557 1.00 10.20 DIC ATOM 201 CA ASP 28 55.119 52.088 58.935 1.00 9.90 DIC ATOM 202 CB ASP 28 56.284 52.933 59.456 1.00 10.34 DIC ATOM 203 CG ASP 28 57.552 52.116 59.643 1.00 10.37 DIC ATOM 204 OD1 ASP 28 57.857 51.288 58.758 1.00 11.78 DIC ATOM 205 OD2 ASP 28 58.241 52.306 60.665 1.00 9.99 DIC ATOM 206 C ASP 28 54.765 51.009 59.951 1.00 11.28 DIC ATOM 207 O ASP 28 55.609 50.577 60.737 1.00 11.87 DIC ATOM 208 N THR 29 53.510 50.576 59.935 1.00 10.17 DIC ATOM 209 CA THR 29 53.062 49.523 60.836 1.00 11.26 DIC ATOM 210 CB THR 29 51.948 50.007 61.791 1.00 9.97 DIC ATOM 211 OG1 THR 29 52.424 51.115 62.566 1.00 10.16 DIC ATOM 212 CG2 THR 29 51.537 48.886 62.737 1.00 10.26 DIC ATOM 213 C THR 29 52.508 48.385 59.992 1.00 11.82 DIC ATOM 214 O THR 29 51.784 48.617 59.022 1.00 11.70 DIC ATOM 215 N GLU 30 52.868 47.159 60.349 1.00 11.89 DIC ATOM 216 CA GLU 30 52.382 45.987 59.632 1.00 14.04 DIC ATOM 217 CB GLU 30 53.142 44.743 60.097 1.00 17.64 DIC ATOM 218 CG GLU 30 53.297 43.655 59.051 1.00 25.15 DIC ATOM 219 CD GLU 30 54.060 44.126 57.822 1.00 27.98 DIC ATOM 220 OE1 GLU 30 53.418 44.612 56.869 1.00 28.55 DIC ATOM 221 OE2 GLU 30 55.306 44.026 57.816 1.00 31.94 DIC ATOM 222 C GLU 30 50.903 45.848 59.982 1.00 12.56 DIC ATOM 223 O GLU 30 50.545 45.798 61.158 1.00 13.85 DIC ATOM 224 N ILE 31 50.041 45.810 58.972 1.00 10.51 DIC ATOM 225 CA ILE 31 48.610 45.666 59.222 1.00 11.18 DIC ATOM 226 CB ILE 31 47.780 46.780 58.526 1.00 11.20 DIC ATOM 227 CG2 ILE 31 46.287 46.575 58.809 1.00 9.63 DIC ATOM 228 CG1 ILE 31 48.218 48.159 59.028 1.00 10.58 DIC ATOM 229 CD ILE 31 47.875 48.435 60.480 1.00 11.64 DIC ATOM 230 C ILE 31 48.142 44.317 58.696 1.00 10.56 DIC ATOM 231 O ILE 31 48.127 44.082 57.487 1.00 11.51 DIC ATOM 232 N ARG 32 47.770 43.430 59.609 1.00 9.50 DIC ATOM 233 CA ARG 32 47.296 42.108 59.227 1.00 9.26 DIC ATOM 234 CB ARG 32 47.919 41.042 60.137 1.00 12.86 DIC ATOM 235 CG ARG 32 49.451 41.101 60.168 1.00 15.87 DIC ATOM 236 CD ARG 32 50.090 39.888 60.831 1.00 19.22 DIC ATOM 237 NE ARG 32 49.697 39.723 62.228 1.00 23.57 DIC ATOM 238 CZ ARG 32 50.227 38.819 63.048 1.00 26.66 DIC ATOM 239 NH1 ARG 32 51.177 38.002 62.608 1.00 27.60 DIC ATOM 240 NH2 ARG 32 49.803 38.723 64.304 1.00 25.75 DIC ATOM 241 C ARG 32 45.774 42.083 59.328 1.00 8.78 DIC ATOM 242 O ARG 32 45.219 42.140 60.426 1.00 6.14 DIC ATOM 243 N PHE 33 45.111 42.021 58.174 1.00 7.42 DIC ATOM 244 CA PHE 33 43.653 41.993 58.107 1.00 6.88 DIC ATOM 245 CB PHE 33 43.159 42.646 56.809 1.00 6.79 DIC ATOM 246 CG PHE 33 43.424 44.126 56.715 1.00 6.63 DIC ATOM 247 CD1 PHE 33 42.732 45.027 57.521 1.00 6.30 DIC ATOM 248 CD2 PHE 33 44.333 44.622 55.784 1.00 6.14 DIC ATOM 249 CE1 PHE 33 42.936 46.403 57.399 1.00 6.64 DIC ATOM 250 CE2 PHE 33 44.548 45.995 55.651 1.00 7.13 DIC ATOM 251 CZ PHE 33 43.845 46.889 56.462 1.00 7.26 DIC ATOM 252 C PHE 33 43.083 40.575 58.175 1.00 7.51 DIC ATOM 253 O PHE 33 43.565 39.662 57.501 1.00 6.94 DIC ATOM 254 N HIS 34 42.048 40.413 58.992 1.00 6.28 DIC ATOM 255 CA HIS 34 41.345 39.141 59.159 1.00 7.93 DIC ATOM 256 CB HIS 34 41.450 38.652 60.604 1.00 8.52 DIC ATOM 257 CG HIS 34 42.855 38.517 61.100 1.00 10.09 DIC ATOM 258 CD2 HIS 34 43.703 39.428 61.632 1.00 11.33 DIC ATOM 259 ND1 HIS 34 43.541 37.322 61.079 1.00 11.33 DIC ATOM 260 CE1 HIS 34 44.751 37.502 61.578 1.00 12.87 DIC ATOM 261 NE2 HIS 34 44.874 38.772 61.921 1.00 11.31 DIC ATOM 262 C HIS 34 39.891 39.483 58.847 1.00 7.56 DIC ATOM 263 O HIS 34 39.260 40.244 59.579 1.00 6.31 DIC ATOM 264 N VAL 35 39.358 38.928 57.766 1.00 6.19 DIC ATOM 265 CA VAL 35 37.990 39.232 57.384 1.00 7.23 DIC ATOM 266 CB VAL 35 37.924 39.665 55.900 1.00 6.63 DIC ATOM 267 CG1 VAL 35 36.498 40.013 55.515 1.00 8.73 DIC ATOM 268 CG2 VAL 35 38.840 40.851 55.669 1.00 8.74 DIC ATOM 269 C VAL 35 37.013 38.081 57.596 1.00 8.74 DIC ATOM 270 O VAL 35 37.174 37.000 57.023 1.00 6.03 DIC ATOM 271 N LEU 36 36.010 38.314 58.438 1.00 7.38 DIC ATOM 272 CA LEU 36 34.984 37.307 58.683 1.00 8.45 DIC ATOM 273 CB LEU 36 34.190 37.639 59.954 1.00 7.92 DIC ATOM 274 CG LEU 36 34.993 37.773 61.259 1.00 8.01 DIC ATOM 275 CD1 LEU 36 34.031 37.960 62.427 1.00 7.60 DIC ATOM 276 CD2 LEU 36 35.847 36.535 61.492 1.00 7.27 DIC ATOM 277 C LEU 36 34.112 37.432 57.432 1.00 9.33 DIC ATOM 278 O LEU 36 33.319 38.365 57.299 1.00 8.93 DIC ATOM 279 N ASP 37 34.304 36.495 56.511 1.00 9.60 DIC ATOM 280 CA ASP 37 33.624 36.471 55.218 1.00 10.03 DIC ATOM 281 CB ASP 37 34.582 35.844 54.199 1.00 11.29 DIC ATOM 282 CG ASP 37 33.980 35.713 52.820 1.00 10.76 DIC ATOM 283 OD1 ASP 37 32.772 35.965 52.659 1.00 10.09 DIC ATOM 284 OD2 ASP 37 34.728 35.344 51.894 1.00 13.51 DIC ATOM 285 C ASP 37 32.287 35.728 55.223 1.00 11.39 DIC ATOM 286 O ASP 37 32.247 34.496 55.212 1.00 9.17 DIC ATOM 287 N ALA 38 31.196 36.489 55.209 1.00 11.46 DIC ATOM 288 CA ALA 38 29.853 35.917 55.230 1.00 13.65 DIC ATOM 289 CB ALA 38 28.914 36.832 56.015 1.00 14.69 DIC ATOM 290 C ALA 38 29.262 35.632 53.851 1.00 14.91 DIC ATOM 291 O ALA 38 28.045 35.490 53.714 1.00 17.68 DIC ATOM 292 N GLY 39 30.111 35.543 52.834 1.00 14.37 DIC ATOM 293 CA GLY 39 29.608 35.255 51.502 1.00 13.29 DIC ATOM 294 C GLY 39 30.109 36.181 50.410 1.00 12.56 DIC ATOM 295 O GLY 39 29.416 36.405 49.421 1.00 13.32 DIC ATOM 296 N ILE 40 31.308 36.724 50.588 1.00 10.63 DIC ATOM 297 CA ILE 40 31.906 37.616 49.597 1.00 9.24 DIC ATOM 298 CB ILE 40 33.142 38.337 50.192 1.00 8.46 DIC ATOM 299 CG2 ILE 40 33.741 39.293 49.168 1.00 7.79 DIC ATOM 300 CG1 ILE 40 32.729 39.099 51.456 1.00 6.53 DIC ATOM 301 CD ILE 40 33.894 39.641 52.273 1.00 9.79 DIC ATOM 302 C ILE 40 32.324 36.806 48.363 1.00 9.40 DIC ATOM 303 O ILE 40 32.951 35.753 48.482 1.00 8.50 DIC ATOM 304 N SER 41 31.972 37.294 47.179 1.00 10.73 DIC ATOM 305 CA SER 41 32.307 36.591 45.942 1.00 11.14 DIC ATOM 306 CB SER 41 31.669 37.295 44.742 1.00 11.01 DIC ATOM 307 OG SER 41 32.317 38.526 44.477 1.00 12.46 DIC ATOM 308 C SER 41 33.816 36.512 45.736 1.00 11.15 DIC ATOM 309 O SER 41 34.569 37.313 46.290 1.00 11.69 DIC ATOM 310 N GLU 42 34.253 35.541 44.940 1.00 12.21 DIC ATOM 311 CA GLU 42 35.673 35.371 44.659 1.00 11.82 DIC ATOM 312 CB GLU 42 35.906 34.153 43.755 1.00 15.43 DIC ATOM 313 CG GLU 42 37.376 33.842 43.483 1.00 19.50 DIC ATOM 314 CD GLU 42 37.989 34.710 42.392 1.00 24.05 DIC ATOM 315 OE1 GLU 42 39.235 34.789 42.331 1.00 27.65 DIC ATOM 316 OE2 GLU 42 37.235 35.302 41.589 1.00 24.25 DIC ATOM 317 C GLU 42 36.199 36.625 43.973 1.00 10.77 DIC ATOM 318 O GLU 42 37.309 37.070 44.248 1.00 9.02 DIC ATOM 319 N ALA 43 35.389 37.193 43.086 1.00 10.24 DIC ATOM 320 CA ALA 43 35.776 38.395 42.359 1.00 11.39 DIC ATOM 321 CB ALA 43 34.720 38.744 41.307 1.00 10.87 DIC ATOM 322 C ALA 43 35.963 39.564 43.317 1.00 10.68 DIC ATOM 323 O ALA 43 36.906 40.343 43.181 1.00 9.26 DIC ATOM 324 N ASN 44 35.070 39.681 44.294 1.00 11.27 DIC ATOM 325 CA ASN 44 35.169 40.774 45.253 1.00 11.66 DIC ATOM 326 CB ASN 44 33.839 40.954 45.997 1.00 10.82 DIC ATOM 327 CG ASN 44 32.789 41.645 45.141 1.00 13.91 DIC ATOM 328 OD1 ASN 44 33.094 42.603 44.429 1.00 14.16 DIC ATOM 329 ND2 ASN 44 31.547 41.171 45.213 1.00 13.53 DIC ATOM 330 C ASN 44 36.326 40.602 46.235 1.00 12.23 DIC ATOM 331 O ASN 44 36.912 41.585 46.686 1.00 12.30 DIC ATOM 332 N ARG 45 36.662 39.358 46.566 1.00 12.83 DIC ATOM 333 CA ARG 45 37.775 39.117 47.477 1.00 13.27 DIC ATOM 334 CB ARG 45 37.838 37.640 47.888 1.00 14.62 DIC ATOM 335 CG ARG 45 36.519 37.103 48.420 1.00 19.99 DIC ATOM 336 CD ARG 45 36.679 36.267 49.680 1.00 23.85 DIC ATOM 337 NE ARG 45 37.610 35.153 49.520 1.00 27.49 DIC ATOM 338 CZ ARG 45 37.746 34.167 50.404 1.00 30.19 DIC ATOM 339 NH1 ARG 45 37.007 34.152 51.506 1.00 31.72 DIC ATOM 340 NH2 ARG 45 38.634 33.202 50.199 1.00 29.60 DIC ATOM 341 C ARG 45 39.063 39.516 46.760 1.00 11.59 DIC ATOM 342 O ARG 45 39.936 40.159 47.337 1.00 8.60 DIC ATOM 343 N ALA 46 39.167 39.141 45.490 1.00 10.34 DIC ATOM 344 CA ALA 46 40.347 39.475 44.704 1.00 10.59 DIC ATOM 345 CB ALA 46 40.257 38.830 43.321 1.00 11.03 DIC ATOM 346 C ALA 46 40.480 40.987 44.567 1.00 10.58 DIC ATOM 347 O ALA 46 41.576 41.535 44.686 1.00 11.52 DIC ATOM 348 N AL A 47 39.360 41.661 44.318 1.00 10.04 DIC ATOM 349 CA ALA 47 39.363 43.112 44.155 1.00 9.25 DIC ATOM 350 CB ALA 47 37.997 43.587 43.672 1.00 11.48 DIC ATOM 351 C ALA 47 39.752 43.844 45.443 1.00 9.33 DIC ATOM 352 O ALA 47 40.459 44.849 45.399 1.00 8.11 DIC ATOM 353 N VAL 48 39.284 43.353 46.587 1.00 9.19 DIC ATOM 354 CA VAL 48 39.624 43.982 47.858 1.00 9.94 DIC ATOM 355 CB VAL 48 38.902 43.302 49.049 1.00 9.44 DIC ATOM 356 CG1 VAL 48 39.431 43.863 50.367 1.00 7.91 DIC ATOM 357 CG2 VAL 48 37.403 43.535 48.955 1.00 6.88 DIC ATOM 358 C VAL 48 41.133 43.867 48.067 1.00 10.57 DIC ATOM 359 O VAL 48 41.808 44.851 48.359 1.00 10.43 DIC ATOM 360 N ALA 49 41.655 42.657 47.898 1.00 11.00 DIC ATOM 361 CA ALA 49 43.079 42.401 48.075 1.00 12.61 DIC ATOM 362 CB ALA 49 43.352 40.903 47.955 1.00 11.98 DIC ATOM 363 C ALA 49 43.951 43.170 47.085 1.00 13.08 DIC ATOM 364 O ALA 49 45.011 43.683 47.446 1.00 13.68 DIC ATOM 365 N ALA 50 43.502 43.251 45.838 1.00 14.66 DIC ATOM 366 CA ALA 50 44.256 43.948 44.801 1.00 14.50 DIC ATOM 367 CB ALA 50 43.530 43.828 43.463 1.00 15.47 DIC ATOM 368 C ALA 50 44.497 45.421 45.132 1.00 15.39 DIC ATOM 369 O ALA 50 45.490 46.004 44.698 1.00 16.30 DIC ATOM 370 N ASN 51 43.590 46.020 45.899 1.00 14.62 DIC ATOM 371 CA ASN 51 43.708 47.429 46.269 1.00 14.05 DIC ATOM 372 CB ASN 51 42.317 48.048 46.439 1.00 12.38 DIC ATOM 373 CG ASN 51 41.634 48.316 45.116 1.00 12.84 DIC ATOM 374 OD1 ASN 51 42.110 49.114 44.314 1.00 13.23 DIC ATOM 375 ND2 ASN 51 40.511 47.651 44.881 1.00 11.33 DIC ATOM 376 C ASN 51 44.512 47.668 47.542 1.00 15.83 DIC ATOM 377 O ASN 51 44.891 48.804 47.841 1.00 17.23 DIC ATOM 378 N LEU 52 44.773 46.607 48.295 1.00 15.52 DIC ATOM 379 CA LEU 52 45.520 46.754 49.535 1.00 17.67 DIC ATOM 380 CB LEU 52 45.106 45.669 50.530 1.00 15.40 DIC ATOM 381 CG LEU 52 43.604 45.719 50.825 1.00 16.03 DIC ATOM 382 CD1 LEU 52 43.233 44.666 51.852 1.00 16.15 DIC ATOM 383 CD2 LEU 52 43.232 47.106 51.322 1.00 15.81 DIC ATOM 384 C LEU 52 47.021 46.730 49.305 1.00 19.77 DIC ATOM 385 O LEU 52 47.497 46.237 48.277 1.00 18.50 DIC ATOM 386 N ARG 53 47.754 47.275 50.271 1.00 21.96 DIC ATOM 387 CA ARG 53 49.207 47.361 50.210 1.00 25.17 DIC ATOM 388 CB ARG 53 49.773 47.572 51.619 1.00 24.25 DIC ATOM 389 CG ARG 53 50.746 48.726 51.703 1.00 23.54 DIC ATOM 390 CD ARG 53 50.512 49.603 52.931 1.00 20.57 DIC ATOM 391 NE ARG 53 50.702 48.882 54.184 1.00 16.68 DIC ATOM 392 CZ ARG 53 50.784 49.472 55.373 1.00 17.69 DIC ATOM 393 NH1 ARG 53 50.694 50.794 55.469 1.00 14.96 DIC ATOM 394 NH2 ARG 53 50.957 48.744 56.467 1.00 16.12 DIC ATOM 395 C ARG 53 49.811 46.124 49.565 1.00 26.76 DIC ATOM 396 O ARG 53 50.790 46.214 48.825 1.00 28.81 DIC ATOM 397 N GLY 55 49.212 44.969 49.834 1.00 28.95 DIC ATOM 398 CA GLY 55 49.702 43.742 49.245 1.00 30.90 DIC ATOM 399 C GLY 55 48.600 42.749 48.919 1.00 32.46 DIC ATOM 400 O GLY 55 48.361 42.412 47.756 1.00 33.41 DIC ATOM 401 N GLY 56 47.909 42.297 49.958 1.00 33.24 DIC ATOM 402 CA GLY 56 46.866 41.306 49.792 1.00 31.87 DIC ATOM 403 C GLY 56 47.421 40.103 50.521 1.00 31.64 DIC ATOM 404 O GLY 56 46.693 39.202 50.943 1.00 32.69 DIC ATOM 405 N GLY 57 48.743 40.105 50.666 1.00 29.97 DIC ATOM 406 CA GLY 57 49.415 39.035 51.373 1.00 28.09 DIC ATOM 407 C GLY 57 49.162 39.249 52.849 1.00 26.72 DIC ATOM 408 O GLY 57 49.474 38.394 53.677 1.00 28.17 DIC ATOM 409 N ASN 58 48.592 40.409 53.171 1.00 24.96 DIC ATOM 410 CA ASN 58 48.272 40.755 54.550 1.00 22.29 DIC ATOM 411 CB ASN 58 48.850 42.121 54.919 1.00 24.14 DIC ATOM 412 CG ASN 58 50.242 42.023 55.510 1.00 27.73 DIC ATOM 413 OD1 ASN 58 50.457 41.332 56.509 1.00 27.14 DIC ATOM 414 ND2 ASN 58 51.198 42.717 54.898 1.00 28.37 DIC ATOM 415 C ASN 58 46.777 40.748 54.832 1.00 19.33 DIC ATOM 416 O ASN 58 46.315 41.409 55.761 1.00 17.00 DIC ATOM 417 N ILE 59 46.016 40.020 54.021 1.00 16.23 DIC ATOM 418 CA ILE 59 44.584 39.920 54.254 1.00 14.14 DIC ATOM 419 CB ILE 59 43.766 40.863 53.329 1.00 15.68 DIC ATOM 420 CG2 ILE 59 43.980 40.502 51.862 1.00 14.29 DIC ATOM 421 CG1 ILE 59 42.283 40.774 53.699 1.00 14.17 DIC ATOM 422 CD ILE 59 41.413 41.795 52.996 1.00 16.56 DIC ATOM 423 C ILE 59 44.133 38.477 54.071 1.00 13.72 DIC ATOM 424 O ILE 59 44.418 37.839 53.056 1.00 12.08 DIC ATOM 425 N ARG 60 43.456 37.953 55.084 1.00 13.05 DIC ATOM 426 CA ARG 60 42.968 36.586 55.031 1.00 12.60 DIC ATOM 427 CB ARG 60 43.685 35.730 56.082 1.00 15.76 DIC ATOM 428 CG ARG 60 43.217 34.284 56.154 1.00 20.30 DIC ATOM 429 CD ARG 60 44.272 33.351 56.769 1.00 24.60 DIC ATOM 430 NE ARG 60 44.682 33.733 58.118 1.00 29.24 DIC ATOM 431 CZ ARG 60 45.606 34.650 58.398 1.00 31.92 DIC ATOM 432 NH1 ARG 60 46.232 35.291 57.419 1.00 34.11 DIC ATOM 433 NH2 ARG 60 45.908 34.926 59.660 1.00 32.11 DIC ATOM 434 C ARG 60 41.469 36.596 55.274 1.00 13.28 DIC ATOM 435 O ARG 60 40.986 37.219 56.225 1.00 12.52 DIC ATOM 436 N PHE 61 40.728 35.932 54.393 1.00 9.98 DIC ATOM 437 CA PHE 61 39.283 35.868 54.543 1.00 11.03 DIC ATOM 438 CB PHE 61 38.593 35.909 53.180 1.00 10.11 DIC ATOM 439 CG PHE 61 38.864 37.165 52.404 1.00 8.69 DIC ATOM 440 CD1 PHE 61 40.001 37.279 51.611 1.00 10.62 DIC ATOM 441 CD2 PHE 61 37.984 38.239 52.470 1.00 8.62 DIC ATOM 442 CE1 PHE 61 40.255 38.444 50.896 1.00 10.15 DIC ATOM 443 CE2 PHE 61 38.231 39.411 51.757 1.00 10.17 DIC ATOM 444 CZ PHE 61 39.368 39.511 50.969 1.00 8.33 DIC ATOM 445 C PHE 61 38.949 34.578 55.265 1.00 10.30 DIC ATOM 446 O PHE 61 39.474 33.520 54.934 1.00 10.02 DIC ATOM 447 N ILE 62 38.080 34.678 56.262 1.00 10.75 DIC ATOM 448 CA ILE 62 37.682 33.525 57.053 1.00 10.78 DIC ATOM 449 CB ILE 62 37.949 33.791 58.550 1.00 11.91 DIC ATOM 450 CG2 ILE 62 37.750 32.516 59.358 1.00 9.27 DIC ATOM 451 CG1 ILE 62 39.380 34.301 58.728 1.00 11.15 DIC ATOM 452 CD ILE 62 39.672 34.864 60.108 1.00 13.99 DIC ATOM 453 C ILE 62 36.199 33.259 56.829 1.00 11.22 DIC ATOM 454 O ILE 62 35.352 34.083 57.172 1.00 8.84 DIC ATOM 455 N ASP 63 35.891 32.102 56.249 1.00 12.77 DIC ATOM 456 CA ASP 63 34.509 31.743 55.963 1.00 15.03 DIC ATOM 457 CB ASP 63 34.450 30.425 55.186 1.00 19.05 DIC ATOM 458 CG ASP 63 35.078 30.533 53.815 1.00 22.78 DIC ATOM 459 OD1 ASP 63 34.633 31.392 53.027 1.00 24.85 DIC ATOM 460 OD2 ASP 63 36.017 29.762 53.526 1.00 26.44 DIC ATOM 461 C ASP 63 33.638 31.624 57.201 1.00 15.28 DIC ATOM 462 O ASP 63 33.989 30.943 58.164 1.00 13.87 DIC ATOM 463 N VAL 64 32.499 32.301 57.170 1.00 14.42 DIC ATOM 464 CA VAL 64 31.558 32.237 58.274 1.00 14.74 DIC ATOM 465 CB VAL 64 31.449 33.587 59.025 1.00 15.80 DIC ATOM 466 CG1 VAL 64 32.778 33.930 59.669 1.00 16.58 DIC ATOM 467 CG2 VAL 64 31.025 34.684 58.073 1.00 16.06 DIC ATOM 468 C VAL 64 30.196 31.865 57.706 1.00 14.22 DIC ATOM 469 O VAL 64 29.826 32.308 56.617 1.00 14.84 DIC ATOM 470 N ASN 65 29.463 31.033 58.435 1.00 12.47 DIC ATOM 471 CA ASN 65 28.137 30.614 58.010 1.00 13.60 DIC ATOM 472 CB ASN 65 27.857 29.182 58.476 1.00 14.16 DIC ATOM 473 CG ASN 65 26.564 28.624 57.906 1.00 16.61 DIC ATOM 474 OD1 ASN 65 25.625 29.367 57.620 1.00 16.00 DIC ATOM 475 ND2 ASN 65 26.505 27.305 57.752 1.00 14.91 DIC ATOM 476 C ASN 65 27.123 31.560 58.647 1.00 14.85 DIC ATOM 477 O ASN 65 26.895 31.510 59.856 1.00 15.54 DIC ATOM 478 N PRO 66 26.509 32.443 57.846 1.00 15.26 DIC ATOM 479 CD PRO 66 26.691 32.671 56.401 1.00 15.57 DIC ATOM 480 CA PRO 66 25.526 33.376 58.404 1.00 15.89 DIC ATOM 481 CB PRO 66 25.166 34.256 57.208 1.00 17.28 DIC ATOM 482 CG PRO 66 25.406 33.358 56.029 1.00 16.80 DIC ATOM 483 C PRO 66 24.311 32.678 59.019 1.00 15.69 DIC ATOM 484 O PRO 66 23.646 33.231 59.893 1.00 16.02 DIC ATOM 485 N ALA 67 24.028 31.461 58.568 1.00 14.83 DIC ATOM 486 CA ALA 67 22.896 30.713 59.101 1.00 15.30 DIC ATOM 487 CB ALA 67 22.749 29.382 58.366 1.00 16.72 DIC ATOM 488 C ALA 67 23.082 30.466 60.597 1.00 15.63 DIC ATOM 489 O ALA 67 22.112 30.252 61.322 1.00 15.80 DIC ATOM 490 N ASP 68 24.330 30.505 61.056 1.00 14.70 DIC ATOM 491 CA ASP 68 24.634 30.282 62.466 1.00 15.13 DIC ATOM 492 CB ASP 68 26.133 30.478 62.736 1.00 15.76 DIC ATOM 493 CG ASP 68 26.987 29.337 62.201 1.00 17.55 DIC ATOM 494 OD1 ASP 68 28.216 29.367 62.418 1.00 17.24 DIC ATOM 495 OD2 ASP 68 26.439 28.415 61.570 1.00 18.46 DIC ATOM 496 C ASP 68 23.854 31.213 63.391 1.00 14.63 DIC ATOM 497 O ASP 68 23.503 30.838 64.507 1.00 15.13 DIC ATOM 498 N PHE 69 23.580 32.424 62.923 1.00 13.83 DIC ATOM 499 CA PHE 69 22.880 33.406 63.740 1.00 14.98 DIC ATOM 500 CB PHE 69 23.691 34.708 63.745 1.00 13.87 DIC ATOM 501 CG PHE 69 25.180 34.484 63.681 1.00 14.17 DIC ATOM 502 CD1 PHE 69 25.823 34.341 62.452 1.00 12.43 DIC ATOM 503 CD2 PHE 69 25.929 34.355 64.847 1.00 12.05 DIC ATOM 504 CE1 PHE 69 27.192 34.071 62.385 1.00 13.43 DIC ATOM 505 CE2 PHE 69 27.297 34.084 64.794 1.00 12.77 DIC ATOM 506 CZ PHE 69 27.932 33.941 63.561 1.00 11.69 DIC ATOM 507 C PHE 69 21.447 33.672 63.285 1.00 15.85 DIC ATOM 508 O PHE 69 20.877 34.719 63.587 1.00 14.86 DIC ATOM 509 N ALA 70 20.863 32.708 62.585 1.00 16.36 DIC ATOM 510 CA ALA 70 19.502 32.840 62.074 1.00 19.02 DIC ATOM 511 CB ALA 70 19.135 31.594 61.269 1.00 20.70 DIC ATOM 512 C ALA 70 18.437 33.095 63.143 1.00 19.98 DIC ATOM 513 O ALA 70 17.366 33.616 62.840 1.00 22.15 DIC ATOM 514 N GLY 71 18.723 32.734 64.388 1.00 18.98 DIC ATOM 515 CA GLY 71 17.740 32.935 65.437 1.00 19.23 DIC ATOM 516 C GLY 71 17.753 34.294 66.114 1.00 19.37 DIC ATOM 517 O GLY 71 16.795 34.653 66.806 1.00 18.55 DIC ATOM 518 N PHE 72 18.824 35.056 65.910 1.00 17.12 DIC ATOM 519 CA PHE 72 18.959 36.370 66.528 1.00 16.52 DIC ATOM 520 CB PHE 72 20.444 36.736 66.627 1.00 17.36 DIC ATOM 521 CG PHE 72 21.244 35.800 67.502 1.00 20.69 DIC ATOM 522 CD1 PHE 72 22.622 35.942 67.615 1.00 20.90 DIC ATOM 523 CD2 PHE 72 20.616 34.781 68.220 1.00 20.65 DIC ATOM 524 CE1 PHE 72 23.365 35.084 68.429 1.00 22.32 DIC ATOM 525 CE2 PHE 72 21.350 33.918 69.036 1.00 21.81 DIC ATOM 526 CZ PHE 72 22.728 34.071 69.139 1.00 22.14 DIC ATOM 527 C PHE 72 18.182 37.476 65.809 1.00 15.69 DIC ATOM 528 O PHE 72 18.062 37.475 64.582 1.00 16.74 DIC ATOM 529 N PRO 73 17.644 38.438 66.576 1.00 14.19 DIC ATOM 530 CD PRO 73 17.784 38.566 68.037 1.00 14.66 DIC ATOM 531 CA PRO 73 16.870 39.558 66.033 1.00 13.58 DIC ATOM 532 CB PRO 73 16.430 40.313 67.287 1.00 14.13 DIC ATOM 533 CG PRO 73 17.522 40.037 68.251 1.00 14.64 DIC ATOM 534 C PRO 73 17.632 40.441 65.053 1.00 13.06 DIC ATOM 535 O PRO 73 18.839 40.647 65.183 1.00 11.47 DIC ATOM 536 N LEU 74 16.912 40.951 64.061 1.00 12.77 DIC ATOM 537 CA LEU 74 17.498 41.819 63.049 1.00 14.73 DIC ATOM 538 CB LEU 74 17.807 40.997 61.793 1.00 16.34 DIC ATOM 539 CG LEU 74 18.987 41.439 60.926 1.00 18.53 DIC ATOM 540 CD1 LEU 74 20.262 41.429 61.767 1.00 15.81 DIC ATOM 541 CD2 LEU 74 19.127 40.503 59.727 1.00 17.94 DIC ATOM 542 C LEU 74 16.493 42.935 62.731 1.00 14.70 DIC ATOM 543 O LEU 74 16.013 43.048 61.603 1.00 17.35 DIC ATOM 544 N ASN 75 16.186 43.758 63.732 1.00 12.80 DIC ATOM 545 CA ASN 75 15.222 44.848 63.573 1.00 11.77 DIC ATOM 546 CB ASN 75 14.595 45.205 64.934 1.00 13.05 DIC ATOM 547 CG ASN 75 15.634 45.441 66.031 1.00 15.54 DIC ATOM 548 OD1 ASN 75 16.359 44.524 66.427 1.00 14.39 DIC ATOM 549 ND2 ASN 75 15.699 46.673 66.533 1.00 13.85 DIC ATOM 550 C ASN 75 15.741 46.122 62.900 1.00 11.45 DIC ATOM 551 O ASN 75 14.947 46.933 62.421 1.00 10.31 DIC ATOM 552 N ILE 76 17.059 46.302 62.865 1.00 9.67 DIC ATOM 553 CA ILE 76 17.649 47.486 62.242 1.00 8.64 DIC ATOM 554 CB ILE 76 18.989 47.859 62.920 1.00 10.45 DIC ATOM 555 CG2 ILE 76 19.526 49.164 62.336 1.00 10.96 DIC ATOM 556 CG1 ILE 76 18.771 48.010 64.433 1.00 11.13 DIC ATOM 557 CD ILE 76 20.026 48.383 65.224 1.00 10.33 DIC ATOM 558 C ILE 76 17.858 47.180 60.761 1.00 6.66 DIC ATOM 559 O ILE 76 18.744 46.417 60.386 1.00 6.82 DIC ATOM 560 N ARG 77 17.022 47.791 59.929 1.00 6.55 DIC ATOM 561 CA ARG 77 17.020 47.565 58.487 1.00 4.60 DIC ATOM 562 CB ARG 77 16.009 48.506 57.830 1.00 6.27 DIC ATOM 563 CG ARG 77 15.689 48.175 56.373 1.00 7.44 DIC ATOM 564 CD ARG 77 14.783 49.243 55.776 1.00 13.42 DIC ATOM 565 NE ARG 77 14.442 48.985 54.379 1.00 15.86 DIC ATOM 566 CZ ARG 77 14.048 49.925 53.525 1.00 17.42 DIC ATOM 567 NH1 ARG 77 13.948 51.184 53.927 1.00 18.20 DIC ATOM 568 NH2 ARG 77 13.755 49.611 52.270 1.00 19.12 DIC ATOM 569 C ARG 77 18.341 47.637 57.727 1.00 5.81 DIC ATOM 570 O ARG 77 18.598 46.795 56.870 1.00 5.17 DIC ATOM 571 N HIS 78 19.182 48.623 58.022 1.00 6.00 DIC ATOM 572 CA HIS 78 20.440 48.744 57.287 1.00 9.02 DIC ATOM 573 CB HIS 78 20.979 50.175 57.389 1.00 10.15 DIC ATOM 574 CG HIS 78 21.474 50.544 58.751 1.00 9.33 DIC ATOM 575 CD2 HIS 78 20.848 51.131 59.797 1.00 6.75 DIC ATOM 576 ND1 HIS 78 22.765 50.293 59.168 1.00 11.81 DIC ATOM 577 CE1 HIS 78 22.911 50.712 60.412 1.00 8.70 DIC ATOM 578 NE2 HIS 78 21.762 51.224 60.817 1.00 11.84 DIC ATOM 579 C HIS 78 21.509 47.751 57.734 1.00 8.20 DIC ATOM 580 O HIS 78 22.624 47.761 57.219 1.00 7.53 DIC ATOM 581 N ILE 79 21.162 46.872 58.669 1.00 7.37 DIC ATOM 582 CA ILE 79 22.129 45.895 59.158 1.00 7.68 DIC ATOM 583 CB ILE 79 22.262 45.979 60.687 1.00 5.65 DIC ATOM 584 CG2 ILE 79 23.256 44.932 61.180 1.00 4.12 DIC ATOM 585 CG1 ILE 79 22.715 47.384 61.083 1.00 4.91 DIC ATOM 586 CD ILE 79 22.696 47.634 62.575 1.00 5.56 DIC ATOM 587 C ILE 79 21.794 44.460 58.783 1.00 8.61 DIC ATOM 588 O ILE 79 20.693 43.983 59.046 1.00 9.77 DIC ATOM 589 N SER 80 22.752 43.773 58.169 1.00 9.76 DIC ATOM 590 CA SER 80 22.561 42.379 57.774 1.00 8.74 DIC ATOM 591 CB SER 80 23.402 42.050 56.541 1.00 8.44 DIC ATOM 592 OG SER 80 24.781 42.091 56.852 1.00 8.55 DIC ATOM 593 C SER 80 22.973 41.462 58.927 1.00 9.00 DIC ATOM 594 O SER 80 23.580 41.913 59.903 1.00 8.52 DIC ATOM 595 N ILE 81 22.637 40.181 58.800 1.00 8.69 DIC ATOM 596 CA ILE 81 22.932 39.167 59.814 1.00 9.32 DIC ATOM 597 CB ILE 81 22.342 37.793 59.391 1.00 11.01 DIC ATOM 598 CG2 ILE 81 23.127 37.231 58.211 1.00 12.45 DIC ATOM 599 CG1 ILE 81 22.387 36.802 60.557 1.00 13.43 DIC ATOM 600 CD ILE 81 21.500 37.182 61.726 1.00 16.17 DIC ATOM 601 C ILE 81 24.433 39.007 60.082 1.00 8.61 DIC ATOM 602 O ILE 81 24.831 38.496 61.123 1.00 9.44 DIC ATOM 603 N THR 82 25.259 39.450 59.144 1.00 8.29 DIC ATOM 604 CA THR 82 26.711 39.346 59.290 1.00 9.90 DIC ATOM 605 CB THR 82 27.416 39.899 58.032 1.00 9.68 DIC ATOM 606 OG1 THR 82 27.081 39.078 56.908 1.00 11.57 DIC ATOM 607 CG2 THR 82 28.924 39.902 58.208 1.00 11.14 DIC ATOM 608 C THR 82 27.226 40.083 60.532 1.00 9.31 DIC ATOM 609 O THR 82 28.308 39.784 61.044 1.00 11.54 DIC ATOM 610 N THR 83 26.442 41.044 61.007 1.00 7.10 DIC ATOM 611 CA THR 83 26.793 41.843 62.178 1.00 6.02 DIC ATOM 612 CB THR 83 25.681 42.891 62.460 1.00 4.53 DIC ATOM 613 OG1 THR 83 26.153 43.855 63.407 1.00 3.63 DIC ATOM 614 CG2 THR 83 24.428 42.217 63.004 1.00 2.50 DIC ATOM 615 C THR 83 27.028 40.992 63.439 1.00 5.43 DIC ATOM 616 O THR 83 27.686 41.435 64.389 1.00 2.82 DIC ATOM 617 N TYR 84 26.490 39.775 63.442 1.00 4.36 DIC ATOM 618 CA TYR 84 26.636 38.865 64.579 1.00 4.81 DIC ATOM 619 CB TYR 84 25.399 37.962 64.707 1.00 5.98 DIC ATOM 620 CG TYR 84 24.158 38.632 65.252 1.00 5.88 DIC ATOM 621 CD1 TYR 84 23.083 38.948 64.415 1.00 7.00 DIC ATOM 622 CE1 TYR 84 21.922 39.534 64.921 1.00 7.41 DIC ATOM 623 CD2 TYR 84 24.040 38.920 66.611 1.00 6.51 DIC ATOM 624 CE2 TYR 84 22.882 39.503 67.129 1.00 6.56 DIC ATOM 625 CZ TYR 84 21.829 39.805 66.277 1.00 7.16 DIC ATOM 626 OH TYR 84 20.682 40.370 66.782 1.00 7.35 DIC ATOM 627 C TYR 84 27.872 37.966 64.507 1.00 5.01 DIC ATOM 628 O TYR 84 28.228 37.317 65.497 1.00 6.35 DIC ATOM 629 N ALA 85 28.524 37.923 63.350 1.00 4.75 DIC ATOM 630 CA ALA 85 29.697 37.068 63.174 1.00 5.04 DIC ATOM 631 CB ALA 85 30.266 37.240 61.765 1.00 5.81 DIC ATOM 632 C ALA 85 30.788 37.323 64.211 1.00 4.45 DIC ATOM 633 O ALA 85 31.506 36.409 64.601 1.00 3.97 DIC ATOM 634 N ARG 86 30.899 38.566 64.663 1.00 5.28 DIC ATOM 635 CA ARG 86 31.918 38.932 65.636 1.00 6.46 DIC ATOM 636 CB ARG 86 31.830 40.436 65.927 1.00 6.54 DIC ATOM 637 CG ARG 86 30.578 40.885 66.662 1.00 7.60 DIC ATOM 638 CD ARG 86 30.479 42.411 66.665 1.00 6.22 DIC ATOM 639 NE ARG 86 29.753 42.918 65.502 1.00 7.60 DIC ATOM 640 CZ ARG 86 29.592 44.209 65.223 1.00 8.07 DIC ATOM 641 NH1 ARG 86 30.121 45.135 66.016 1.00 6.32 DIC ATOM 642 NH2 ARG 86 28.866 44.578 64.173 1.00 6.28 DIC ATOM 643 C ARG 86 31.834 38.123 66.933 1.00 6.26 DIC ATOM 644 O ARG 86 32.825 37.970 67.642 1.00 5.75 DIC ATOM 645 N LEU 87 30.654 37.594 67.231 1.00 6.67 DIC ATOM 646 CA LEU 87 30.453 36.800 68.444 1.00 9.15 DIC ATOM 647 CB LEU 87 28.978 36.423 68.579 1.00 9.79 DIC ATOM 648 CG LEU 87 27.968 37.573 68.662 1.00 10.81 DIC ATOM 649 CD1 LEU 87 26.565 36.998 68.625 1.00 10.16 DIC ATOM 650 CD2 LEU 87 28.186 38.385 69.928 1.00 9.69 DIC ATOM 651 C LEU 87 31.309 35.531 68.500 1.00 8.69 DIC ATOM 652 O LEU 87 31.663 35.069 69.583 1.00 8.91 DIC ATOM 653 N LYS 88 31.633 34.964 67.337 1.00 9.25 DIC ATOM 654 CA LYS 88 32.453 33.749 67.269 1.00 7.47 DIC ATOM 655 CB LYS 88 31.882 32.787 66.215 1.00 8.55 DIC ATOM 656 CG LYS 88 30.591 32.084 66.618 1.00 5.05 DIC ATOM 657 CD LYS 88 30.239 31.000 65.605 1.00 9.57 DIC ATOM 658 CE LYS 88 29.127 30.091 66.111 1.00 11.92 DIC ATOM 659 NZ LYS 88 28.966 28.889 65.234 1.00 9.27 DIC ATOM 660 C LYS 88 33.921 34.034 66.932 1.00 8.56 DIC ATOM 661 O LYS 88 34.635 33.166 66.426 1.00 7.98 DIC ATOM 662 N LEU 89 34.374 35.247 67.221 1.00 8.21 DIC ATOM 663 CA LEU 89 35.746 35.638 66.924 1.00 9.63 DIC ATOM 664 CB LEU 89 35.968 37.079 67.392 1.00 11.64 DIC ATOM 665 CG LEU 89 36.996 37.961 66.683 1.00 15.58 DIC ATOM 666 CD1 LEU 89 36.916 37.802 65.176 1.00 14.23 DIC ATOM 667 CD2 LEU 89 36.731 39.405 67.074 1.00 15.43 DIC ATOM 668 C LEU 89 36.760 34.688 67.564 1.00 10.10 DIC ATOM 669 O LEU 89 37.825 34.423 66.998 1.00 10.90 DIC ATOM 670 N GLY 90 36.420 34.165 68.738 1.00 8.62 DIC ATOM 671 CA GLY 90 37.306 33.238 69.422 1.00 9.71 DIC ATOM 672 C GLY 90 37.439 31.920 68.679 1.00 10.61 DIC ATOM 673 O GLY 90 38.417 31.195 68.858 1.00 9.41 DIC ATOM 674 N GLU 91 36.447 31.607 67.848 1.00 9.92 DIC ATOM 675 CA GLU 91 36.453 30.379 67.058 1.00 11.25 DIC ATOM 676 CB GLU 91 35.022 29.875 66.839 1.00 14.13 DIC ATOM 677 CG GLU 91 34.281 29.413 68.084 1.00 17.36 DIC ATOM 678 CD GLU 91 32.897 28.871 67.750 1.00 20.17 DIC ATOM 679 OE1 GLU 91 32.791 28.072 66.794 1.00 19.66 DIC ATOM 680 OE2 GLU 91 31.921 29.234 68.441 1.00 19.51 DIC ATOM 681 C GLU 91 37.093 30.594 65.683 1.00 11.62 DIC ATOM 682 O GLU 91 37.663 29.664 65.100 1.00 11.92 DIC ATOM 683 N TYR 92 36.989 31.819 65.173 1.00 10.48 DIC ATOM 684 CA TYR 92 37.516 32.165 63.854 1.00 10.15 DIC ATOM 685 CB TYR 92 36.725 33.331 63.253 1.00 9.65 DIC ATOM 686 CG TYR 92 35.244 33.078 63.086 1.00 11.40 DIC ATOM 687 CD1 TYR 92 34.774 31.872 62.568 1.00 10.51 DIC ATOM 688 CE1 TYR 92 33.411 31.655 62.371 1.00 13.36 DIC ATOM 689 CD2 TYR 92 34.312 34.066 63.406 1.00 11.86 DIC ATOM 690 CE2 TYR 92 32.948 33.861 63.211 1.00 13.22 DIC ATOM 691 CZ TYR 92 32.505 32.654 62.695 1.00 14.23 DIC ATOM 692 OH TYR 92 31.159 32.447 62.507 1.00 12.62 DIC ATOM 693 C TYR 92 38.992 32.518 63.776 1.00 10.04 DIC ATOM 694 O TYR 92 39.601 32.361 62.723 1.00 9.17 DIC ATOM 695 N ILE 93 39.563 33.014 64.870 1.00 11.91 DIC ATOM 696 CA ILE 93 40.971 33.405 64.886 1.00 13.98 DIC ATOM 697 CB ILE 93 41.122 34.938 65.044 1.00 15.92 DIC ATOM 698 CG2 ILE 93 42.597 35.318 65.098 1.00 14.58 DIC ATOM 699 CG1 ILE 93 40.441 35.650 63.872 1.00 16.29 DIC ATOM 700 CD ILE 93 40.462 37.154 63.985 1.00 14.93 DIC ATOM 701 C ILE 93 41.728 32.721 66.018 1.00 15.16 DIC ATOM 702 O ILE 93 41.350 32.830 67.185 1.00 14.37 DIC ATOM 703 N ALA 94 42.804 32.028 65.663 1.00 14.83 DIC ATOM 704 CA ALA 94 43.608 31.305 66.639 1.00 19.11 DIC ATOM 705 CB ALA 94 43.703 29.845 66.231 1.00 19.20 DIC ATOM 706 C ALA 94 45.013 31.871 66.836 1.00 19.59 DIC ATOM 707 O ALA 94 45.592 31.747 67.915 1.00 20.84 DIC ATOM 708 N ASP 95 45.552 32.493 65.794 1.00 21.87 DIC ATOM 709 CA ASP 95 46.905 33.044 65.831 1.00 23.46 DIC ATOM 710 CB ASP 95 47.409 33.251 64.397 1.00 26.41 DIC ATOM 711 CG ASP 95 46.424 34.024 63.537 1.00 29.30 DIC ATOM 712 OD1 ASP 95 46.717 34.258 62.344 1.00 32.19 DIC ATOM 713 OD2 ASP 95 45.351 34.398 64.050 1.00 33.42 DIC ATOM 714 C ASP 95 47.115 34.332 66.626 1.00 22.72 DIC ATOM 715 O ASP 95 48.257 34.737 66.851 1.00 24.34 DIC ATOM 716 N CYS 96 46.036 34.968 67.069 1.00 21.07 DIC ATOM 717 CA CYS 96 46.168 36.221 67.811 1.00 19.00 DIC ATOM 718 CB CYS 96 45.485 37.356 67.043 1.00 17.51 DIC ATOM 719 SG CYS 96 46.000 37.495 65.337 1.00 17.81 DIC ATOM 720 C CYS 96 45.603 36.192 69.223 1.00 17.30 DIC ATOM 721 O CYS 96 44.532 35.636 69.459 1.00 18.98 DIC ATOM 722 N ASP 97 46.326 36.804 70.155 1.00 15.20 DIC ATOM 723 CA ASP 97 45.879 36.886 71.540 1.00 15.33 DIC ATOM 724 CB ASP 97 47.070 36.957 72.495 1.00 16.39 DIC ATOM 725 CG ASP 97 47.696 35.605 72.741 1.00 17.76 DIC ATOM 726 OD1 ASP 97 48.786 35.559 73.347 1.00 22.14 DIC ATOM 727 OD2 ASP 97 47.091 34.590 72.335 1.00 18.91 DIC ATOM 728 C ASP 97 45.041 38.146 71.689 1.00 14.04 DIC ATOM 729 O ASP 97 44.289 38.297 72.652 1.00 13.55 DIC ATOM 730 N ALA 98 45.192 39.051 70.728 1.00 12.61 DIC ATOM 731 CA ALA 98 44.457 40.309 70.727 1.00 12.75 DIC ATOM 732 CB ALA 98 45.220 41.362 71.513 1.00 14.90 DIC ATOM 733 C ALA 98 44.243 40.786 69.299 1.00 10.95 DIC ATOM 734 O ALA 98 45.130 40.664 68.456 1.00 10.19 DIC ATOM 735 N VAL 99 43.055 41.317 69.032 1.00 9.01 DIC ATOM 736 CA VAL 99 42.726 41.827 67.710 1.00 8.36 DIC ATOM 737 CB VAL 99 41.911 40.801 66.883 1.00 7.71 DIC ATOM 738 CG1 VAL 99 42.761 39.579 66.590 1.00 4.15 DIC ATOM 739 CG2 VAL 99 40.639 40.407 67.637 1.00 5.20 DIC ATOM 740 C VAL 99 41.902 43.090 67.862 1.00 8.06 DIC ATOM 741 O VAL 99 41.233 43.282 68.877 1.00 8.30 DIC ATOM 742 N LEU 100 41.965 43.961 66.864 1.00 6.36 DIC ATOM 743 CA LEU 100 41.193 45.193 66.905 1.00 5.80 DIC ATOM 744 CB LEU 100 42.084 46.407 66.611 1.00 5.45 DIC ATOM 745 CG LEU 100 41.418 47.790 66.524 1.00 8.26 DIC ATOM 746 CD1 LEU 100 40.403 47.975 67.641 1.00 6.61 DIC ATOM 747 CD2 LEU 100 42.492 48.867 66.602 1.00 8.45 DIC ATOM 748 C LEU 100 40.092 45.086 65.867 1.00 5.59 DIC ATOM 749 O LEU 100 40.352 45.145 64.663 1.00 5.35 DIC ATOM 750 N TYR 101 38.864 44.910 66.343 1.00 4.71 DIC ATOM 751 CA TYR 101 37.720 44.795 65.462 1.00 5.45 DIC ATOM 752 CB TYR 101 36.624 43.930 66.105 1.00 7.22 DIC ATOM 753 CG TYR 101 35.306 44.030 65.366 1.00 6.26 DIC ATOM 754 CD1 TYR 101 34.459 45.119 65.565 1.00 10.55 DIC ATOM 755 CE1 TYR 101 33.308 45.290 64.805 1.00 11.37 DIC ATOM 756 CD2 TYR 101 34.957 43.099 64.390 1.00 9.90 DIC ATOM 757 CE2 TYR 101 33.799 43.261 63.622 1.00 10.47 DIC ATOM 758 CZ TYR 101 32.987 44.361 63.834 1.00 10.64 DIC ATOM 759 OH TYR 101 31.868 44.565 63.051 1.00 16.19 DIC ATOM 760 C TYR 101 37.142 46.160 65.101 1.00 5.61 DIC ATOM 761 O TYR 101 36.947 47.020 65.968 1.00 4.16 DIC ATOM 762 N LEU 102 36.857 46.339 63.816 1.00 4.05 DIC ATOM 763 CA LEU 102 36.279 47.580 63.314 1.00 4.38 DIC ATOM 764 CB LEU 102 37.295 48.338 62.462 1.00 4.30 DIC ATOM 765 CG LEU 102 38.591 48.754 63.147 1.00 7.19 DIC ATOM 766 CD1 LEU 102 39.510 49.400 62.128 1.00 6.72 DIC ATOM 767 CD2 LEU 102 38.276 49.714 64.293 1.00 3.87 DIC ATOM 768 C LEU 102 35.061 47.286 62.451 1.00 4.47 DIC ATOM 769 O LEU 102 35.034 46.284 61.733 1.00 4.61 DIC ATOM 770 N ASP 103 34.054 48.153 62.534 1.00 3.95 DIC ATOM 771 CA ASP 103 32.860 48.016 61.715 1.00 4.24 DIC ATOM 772 CB ASP 103 31.761 48.979 62.177 1.00 2.65 DIC ATOM 773 CG ASP 103 30.737 48.327 63.095 1.00 2.68 DIC ATOM 774 OD1 ASP 103 29.754 49.012 63.436 1.00 4.76 DIC ATOM 775 OD2 ASP 103 30.897 47.152 63.482 1.00 3.70 DIC ATOM 776 C ASP 103 33.328 48.428 60.320 1.00 5.01 DIC ATOM 777 O ASP 103 34.417 48.975 60.169 1.00 3.63 DIC ATOM 778 N ILE 104 32.507 48.184 59.310 1.00 6.60 DIC ATOM 779 CA ILE 104 32.867 48.531 57.935 1.00 5.92 DIC ATOM 780 CB ILE 104 32.014 47.723 56.933 1.00 6.60 DIC ATOM 781 CG2 ILE 104 32.269 48.202 55.505 1.00 5.47 DIC ATOM 782 CG1 ILE 104 32.308 46.229 57.092 1.00 6.21 DIC ATOM 783 CD ILE 104 33.753 45.837 56.829 1.00 6.76 DIC ATOM 784 C ILE 104 32.675 50.018 57.655 1.00 6.14 DIC ATOM 785 O ILE 104 33.386 50.610 56.838 1.00 6.24 DIC ATOM 786 N ASP 105 31.712 50.618 58.344 1.00 4.96 DIC ATOM 787 CA ASP 105 31.399 52.028 58.167 1.00 5.98 DIC ATOM 788 CB ASP 105 29.930 52.274 58.513 1.00 4.82 DIC ATOM 789 CG ASP 105 29.609 51.925 59.956 1.00 3.16 DIC ATOM 790 OD1 ASP 105 30.337 51.092 60.532 1.00 2.79 DIC ATOM 791 OD2 ASP 105 28.627 52.466 60.507 1.00 5.38 DIC ATOM 792 C ASP 105 32.286 52.943 59.009 1.00 6.62 DIC ATOM 793 O ASP 105 31.790 53.838 59.693 1.00 6.81 DIC ATOM 794 N VAL 106 33.594 52.710 58.966 1.00 7.03 DIC ATOM 795 CA VAL 106 34.536 53.540 59.706 1.00 7.28 DIC ATOM 796 CB VAL 106 35.300 52.752 60.801 1.00 8.49 DIC ATOM 797 CG1 VAL 106 34.321 52.057 61.732 1.00 7.70 DIC ATOM 798 CG2 VAL 106 36.257 51.754 60.156 1.00 8.17 DIC ATOM 799 C VAL 106 35.575 54.126 58.761 1.00 6.79 DIC ATOM 800 O VAL 106 35.848 53.586 57.684 1.00 5.38 DIC ATOM 801 N LEU 107 36.151 55.243 59.180 1.00 7.44 DIC ATOM 802 CA LEU 107 37.179 55.916 58.410 1.00 9.27 DIC ATOM 803 CB LEU 107 36.598 57.173 57.756 1.00 11.52 DIC ATOM 804 CG LEU 107 36.654 57.330 56.232 1.00 15.69 DIC ATOM 805 CD1 LEU 107 36.132 56.088 55.542 1.00 17.09 DIC ATOM 806 CD2 LEU 107 35.829 58.543 55.834 1.00 16.31 DIC ATOM 807 C LEU 107 38.239 56.284 59.441 1.00 8.22 DIC ATOM 808 O LEU 107 38.038 57.190 60.241 1.00 8.43 DIC ATOM 809 N VAL 108 39.346 55.548 59.447 1.00 9.38 DIC ATOM 810 CA VAL 108 40.429 55.812 60.390 1.00 9.80 DIC ATOM 811 CB VAL 108 41.415 54.627 60.456 1.00 8.32 DIC ATOM 812 CG1 VAL 108 42.534 54.927 61.462 1.00 7.62 DIC ATOM 813 CG2 VAL 108 40.667 53.368 60.857 1.00 8.96 DIC ATOM 814 C VAL 108 41.165 57.056 59.926 1.00 11.09 DIC ATOM 815 O VAL 108 41.661 57.100 58.801 1.00 11.19 DIC ATOM 816 N ARG 109 41.234 58.061 60.794 1.00 11.01 DIC ATOM 817 CA ARG 109 41.879 59.327 60.453 1.00 12.38 DIC ATOM 818 CB ARG 109 40.927 60.487 60.743 1.00 14.98 DIC ATOM 819 CG ARG 109 39.453 60.116 60.700 1.00 19.75 DIC ATOM 820 CD ARG 109 38.650 61.137 59.922 1.00 23.34 DIC ATOM 821 NE ARG 109 39.023 62.512 60.241 1.00 26.83 DIC ATOM 822 CZ ARG 109 38.634 63.568 59.529 1.00 28.43 DIC ATOM 823 NH1 ARG 109 39.017 64.789 59.879 1.00 28.45 DIC ATOM 824 NH2 ARG 109 37.862 63.400 58.462 1.00 27.61 DIC ATOM 825 C ARG 109 43.197 59.582 61.181 1.00 12.26 DIC ATOM 826 O ARG 109 43.930 60.511 60.836 1.00 12.24 DIC ATOM 827 N ASP 110 43.484 58.780 62.201 1.00 10.65 DIC ATOM 828 CA ASP 110 44.723 58.934 62.954 1.00 10.25 DIC ATOM 829 CB ASP 110 44.519 59.891 64.140 1.00 11.53 DIC ATOM 830 CG ASP 110 45.831 60.491 64.648 1.00 16.88 DIC ATOM 831 OD1 ASP 110 46.727 60.759 63.819 1.00 17.49 DIC ATOM 832 OD2 ASP 110 45.962 60.717 65.873 1.00 16.60 DIC ATOM 833 C ASP 110 45.160 57.560 63.436 1.00 10.59 DIC ATOM 834 O ASP 110 44.371 56.613 63.457 1.00 9.32 DIC ATOM 835 N ARG 111 46.426 57.455 63.817 1.00 10.81 DIC ATOM 836 CA ARG 111 46.983 56.199 64.279 1.00 9.88 DIC ATOM 837 CB ARG 111 48.427 56.420 64.706 1.00 13.67 DIC ATOM 838 CG ARG 111 49.043 55.233 65.361 1.00 12.82 DIC ATOM 839 CD ARG 111 49.542 55.638 66.719 1.00 24.99 DIC ATOM 840 NE ARG 111 50.595 56.646 66.660 1.00 28.05 DIC ATOM 841 CZ ARG 111 51.187 57.155 67.733 1.00 29.20 DIC ATOM 842 NH1 ARG 111 50.825 56.747 68.943 1.00 29.64 DIC ATOM 843 NH2 ARG 111 52.141 58.069 67.597 1.00 32.61 DIC ATOM 844 C ARG 111 46.201 55.533 65.410 1.00 9.74 DIC ATOM 845 O ARG 111 45.718 56.189 66.330 1.00 6.00 DIC ATOM 846 N LEU 112 46.097 54.211 65.330 1.00 7.64 DIC ATOM 847 CA LEU 112 45.381 53.419 66.322 1.00 7.15 DIC ATOM 848 CB LEU 112 44.572 52.328 65.613 1.00 7.72 DIC ATOM 849 CG LEU 112 43.132 52.585 65.149 1.00 11.87 DIC ATOM 850 CD1 LEU 112 42.820 54.067 65.067 1.00 11.31 DIC ATOM 851 CD2 LEU 112 42.934 51.891 63.815 1.00 12.19 DIC ATOM 852 C LEU 112 46.294 52.759 67.358 1.00 6.68 DIC ATOM 853 O LEU 112 45.812 52.069 68.256 1.00 5.47 DIC ATOM 854 N THR 113 47.601 52.968 67.262 1.00 6.84 DIC ATOM 855 CA THR 113 48.491 52.305 68.211 1.00 9.74 DIC ATOM 856 CB THR 113 49.982 52.542 67.867 1.00 13.43 DIC ATOM 857 OG1 THR 113 50.395 53.834 68.316 1.00 20.21 DIC ATOM 858 CG2 THR 113 50.191 52.430 66.366 1.00 9.16 DIC ATOM 859 C THR 113 48.233 52.627 69.686 1.00 9.89 DIC ATOM 860 O THR 113 48.456 51.780 70.549 1.00 10.39 DIC ATOM 861 N PRO 114 47.763 53.847 70.005 1.00 10.53 DIC ATOM 862 CD PRO 114 47.662 55.093 69.228 1.00 10.25 DIC ATOM 863 CA PRO 114 47.521 54.104 71.428 1.00 9.66 DIC ATOM 864 CB PRO 114 47.058 55.558 71.440 1.00 10.92 DIC ATOM 865 CG PRO 114 47.832 56.151 70.300 1.00 12.85 DIC ATOM 866 C PRO 114 46.445 53.146 71.932 1.00 8.05 DIC ATOM 867 O PRO 114 46.529 52.620 73.039 1.00 6.80 DIC ATOM 868 N LEU 115 45.432 52.918 71.103 1.00 7.04 DIC ATOM 869 CA LEU 115 44.353 52.008 71.467 1.00 8.26 DIC ATOM 870 CB LEU 115 43.193 52.130 70.472 1.00 6.84 DIC ATOM 871 CG LEU 115 42.014 51.170 70.661 1.00 8.47 DIC ATOM 872 CD1 LEU 115 41.399 51.358 72.036 1.00 8.73 DIC ATOM 873 CD2 LEU 115 40.980 51.430 69.568 1.00 11.14 DIC ATOM 874 C LEU 115 44.897 50.582 71.471 1.00 5.85 DIC ATOM 875 O LEU 115 44.663 49.821 72.407 1.00 10.05 DIC ATOM 876 N TRP 116 45.634 50.238 70.422 1.00 6.30 DIC ATOM 877 CA TRP 116 46.233 48.914 70.284 1.00 7.03 DIC ATOM 878 CB TRP 116 47.005 48.836 68.962 1.00 5.84 DIC ATOM 879 CG TRP 116 47.720 47.527 68.737 1.00 8.60 DIC ATOM 880 CD2 TRP 116 47.120 46.266 68.423 1.00 7.22 DIC ATOM 881 CE2 TRP 116 48.165 45.319 68.322 1.00 8.24 DIC ATOM 882 CE3 TRP 116 45.797 45.841 68.221 1.00 7.76 DIC ATOM 883 CD1 TRP 116 49.067 47.303 68.810 1.00 8.45 DIC ATOM 884 NE1 TRP 116 49.342 45.980 68.562 1.00 8.62 DIC ATOM 885 CZ2 TRP 116 47.933 43.973 68.024 1.00 7.56 DIC ATOM 886 CZ3 TRP 116 45.565 44.501 67.923 1.00 9.68 DIC ATOM 887 CH2 TRP 116 46.632 43.581 67.829 1.00 9.41 DIC ATOM 888 C TRP 116 47.165 48.584 71.455 1.00 8.65 DIC ATOM 889 O TRP 116 47.199 47.448 71.926 1.00 8.41 DIC ATOM 890 N ASP 117 47.907 49.582 71.932 1.00 10.05 DIC ATOM 891 CA ASP 117 48.841 49.373 73.038 1.00 10.53 DIC ATOM 892 CB ASP 117 49.912 50.474 73.063 1.00 9.66 DIC ATOM 893 CG ASP 117 50.846 50.423 71.863 1.00 12.25 DIC ATOM 894 OD1 ASP 117 51.014 49.337 71.266 1.00 8.12 DIC ATOM 895 OD2 ASP 117 51.434 51.476 71.529 1.00 10.94 DIC ATOM 896 C ASP 117 48.168 49.313 74.409 1.00 12.03 DIC ATOM 897 O ASP 117 48.827 49.044 75.415 1.00 11.16 DIC ATOM 898 N THR 118 46.862 49.564 74.457 1.00 12.84 DIC ATOM 899 CA THR 118 46.141 49.536 75.727 1.00 13.69 DIC ATOM 900 CB THR 118 44.652 49.929 75.542 1.00 13.94 DIC ATOM 901 OG1 THR 118 44.568 51.266 75.027 1.00 13.81 DIC ATOM 902 CG2 THR 118 43.913 49.864 76.871 1.00 13.09 DIC ATOM 903 C THR 118 46.212 48.148 76.359 1.00 15.13 DIC ATOM 904 O THR 118 46.004 47.137 75.683 1.00 13.70 DIC ATOM 905 N ASP 119 46.523 48.102 77.652 1.00 16.15 DIC ATOM 906 CA ASP 119 46.608 46.831 78.368 1.00 18.15 DIC ATOM 907 CB ASP 119 47.565 46.945 79.557 1.00 22.51 DIC ATOM 908 CG ASP 119 47.891 45.597 80.177 1.00 26.80 DIC ATOM 909 OD1 ASP 119 46.976 44.757 80.303 1.00 29.43 DIC ATOM 910 OD2 ASP 119 49.064 45.378 80.549 1.00 32.86 DIC ATOM 911 C ASP 119 45.208 46.483 78.869 1.00 17.06 DIC ATOM 912 O ASP 119 44.670 47.164 79.740 1.00 16.61 DIC ATOM 913 N LEU 120 44.628 45.424 78.314 1.00 15.39 DIC ATOM 914 CA LEU 120 43.281 44.997 78.681 1.00 15.18 DIC ATOM 915 CB LEU 120 42.688 44.134 77.562 1.00 14.33 DIC ATOM 916 CG LEU 120 42.345 44.801 76.223 1.00 13.88 DIC ATOM 917 CD1 LEU 120 43.564 45.510 75.668 1.00 17.27 DIC ATOM 918 CD2 LEU 120 41.852 43.749 75.243 1.00 12.16 DIC ATOM 919 C LEU 120 43.205 44.227 79.998 1.00 15.94 DIC ATOM 920 O LEU 120 42.117 44.031 80.541 1.00 16.09 DIC ATOM 921 N GLY 121 44.349 43.789 80.513 1.00 15.28 DIC ATOM 922 CA GLY 121 44.329 43.033 81.752 1.00 16.86 DIC ATOM 923 C GLY 121 43.407 41.838 81.581 1.00 17.04 DIC ATOM 924 O GLY 121 43.440 41.174 80.542 1.00 16.37 DIC ATOM 925 N ASN 122 42.575 41.563 82.578 1.00 16.91 DIC ATOM 926 CA ASN 122 41.659 40.433 82.486 1.00 17.19 DIC ATOM 927 CB ASN 122 41.549 39.714 83.835 1.00 20.20 DIC ATOM 928 CG ASN 122 40.814 38.386 83.729 1.00 23.09 DIC ATOM 929 OD1 ASN 122 41.147 37.543 82.892 1.00 25.09 DIC ATOM 930 ND2 ASN 122 39.813 38.193 84.582 1.00 25.01 DIC ATOM 931 C ASN 122 40.275 40.868 82.014 1.00 15.72 DIC ATOM 932 O ASN 122 39.290 40.151 82.204 1.00 14.86 DIC ATOM 933 N ASN 123 40.201 42.053 81.415 1.00 13.48 DIC ATOM 934 CA ASN 123 38.937 42.556 80.891 1.00 12.64 DIC ATOM 935 CB ASN 123 39.026 44.057 80.579 1.00 12.19 DIC ATOM 936 CG ASN 123 39.078 44.921 81.831 1.00 15.92 DIC ATOM 937 OD1 ASN 123 40.093 45.563 82.122 1.00 15.70 DIC ATOM 938 ND2 ASN 123 37.983 44.940 82.576 1.00 13.08 DIC ATOM 939 C ASN 123 38.657 41.791 79.600 1.00 11.07 DIC ATOM 940 O ASN 123 39.582 41.276 78.971 1.00 10.73 DIC ATOM 941 N TRP 124 37.386 41.721 79.212 1.00 11.13 DIC ATOM 942 CA TRP 124 36.988 41.025 77.991 1.00 8.79 DIC ATOM 943 CB TRP 124 35.477 40.814 77.965 1.00 9.02 DIC ATOM 944 CG TRP 124 34.945 39.904 79.021 1.00 9.43 DIC ATOM 945 CD2 TRP 124 34.870 38.478 78.954 1.00 9.01 DIC ATOM 946 CE2 TRP 124 34.238 38.035 80.140 1.00 9.81 DIC ATOM 947 CE3 TRP 124 35.274 37.527 78.005 1.00 8.70 DIC ATOM 948 CD1 TRP 124 34.378 40.264 80.213 1.00 9.23 DIC ATOM 949 NE1 TRP 124 33.947 39.145 80.890 1.00 9.23 DIC ATOM 950 CZ2 TRP 124 33.997 36.681 80.401 1.00 9.69 DIC ATOM 951 CZ3 TRP 124 35.033 36.179 78.266 1.00 9.36 DIC ATOM 952 CH2 TRP 124 34.400 35.772 79.456 1.00 9.63 DIC ATOM 953 C TRP 124 37.381 41.804 76.735 1.00 8.82 DIC ATOM 954 O TRP 124 37.742 41.218 75.712 1.00 7.06 DIC ATOM 955 N LEU 125 37.294 43.125 76.812 1.00 7.98 DIC ATOM 956 CA LEU 125 37.630 43.966 75.669 1.00 9.33 DIC ATOM 957 CB LEU 125 36.580 43.793 74.563 1.00 7.77 DIC ATOM 958 CG LEU 125 35.173 44.370 74.791 1.00 11.95 DIC ATOM 959 CD1 LEU 125 34.233 43.857 73.703 1.00 11.77 DIC ATOM 960 CD2 LEU 125 34.641 43.968 76.154 1.00 15.27 DIC ATOM 961 C LEU 125 37.701 45.437 76.055 1.00 9.18 DIC ATOM 962 O LEU 125 37.325 45.826 77.160 1.00 9.87 DIC ATOM 963 N GLY 126 38.202 46.240 75.127 1.00 8.36 DIC ATOM 964 CA GLY 126 38.291 47.667 75.333 1.00 9.63 DIC ATOM 965 C GLY 126 37.379 48.269 74.284 1.00 9.92 DIC ATOM 966 O GLY 126 37.397 47.838 73.128 1.00 8.79 DIC ATOM 967 N ALA 127 36.566 49.243 74.674 1.00 8.77 DIC ATOM 968 CA ALA 127 35.650 49.870 73.726 1.00 7.45 DIC ATOM 969 CB ALA 127 34.386 49.022 73.594 1.00 7.33 DIC ATOM 970 C ALA 127 35.284 51.290 74.145 1.00 8.08 DIC ATOM 971 O ALA 127 35.462 51.675 75.305 1.00 5.69 DIC ATOM 972 N SER 128 34.787 52.069 73.189 1.00 6.63 DIC ATOM 973 CA SER 128 34.383 53.441 73.461 1.00 7.92 DIC ATOM 974 CB SER 128 34.631 54.327 72.233 1.00 8.31 DIC ATOM 975 OG SER 128 36.021 54.413 71.932 1.00 7.53 DIC ATOM 976 C SER 128 32.905 53.452 73.843 1.00 7.98 DIC ATOM 977 O SER 128 32.129 52.605 73.390 1.00 6.12 DIC ATOM 978 N ILE 129 32.529 54.411 74.683 1.00 8.45 DIC ATOM 979 CA ILE 129 31.157 54.547 75.165 1.00 7.19 DIC ATOM 980 CB ILE 129 31.110 55.479 76.406 1.00 8.54 DIC ATOM 981 CG2 ILE 129 29.667 55.842 76.752 1.00 9.06 DIC ATOM 982 CG1 ILE 129 31.815 54.799 77.586 1.00 8.78 DIC ATOM 983 CD ILE 129 31.972 55.685 78.804 1.00 8.26 DIC ATOM 984 C ILE 129 30.205 55.092 74.104 1.00 8.79 DIC ATOM 985 O ILE 129 30.572 55.954 73.305 1.00 6.50 DIC ATOM 986 N ASP 130 28.980 54.577 74.100 1.00 7.31 DIC ATOM 987 CA ASP 130 27.978 55.037 73.152 1.00 8.69 DIC ATOM 988 CB ASP 130 27.102 53.873 72.692 1.00 6.90 DIC ATOM 989 CG ASP 130 26.237 54.238 71.510 1.00 7.79 DIC ATOM 990 OD1 ASP 130 25.535 55.274 71.578 1.00 7.38 DIC ATOM 991 OD2 ASP 130 26.258 53.493 70.511 1.00 8.54 DIC ATOM 992 C ASP 130 27.125 56.078 73.871 1.00 8.24 DIC ATOM 993 O ASP 130 26.249 55.729 74.660 1.00 9.03 DIC ATOM 994 N LEU 131 27.398 57.353 73.608 1.00 10.56 DIC ATOM 995 CA LEU 131 26.668 58.456 74.242 1.00 11.56 DIC ATOM 996 CB LEU 131 27.234 59.808 73.785 1.00 11.69 DIC ATOM 997 CG LEU 131 28.607 60.232 74.318 1.00 15.03 DIC ATOM 998 CD1 LEU 131 29.662 59.190 73.969 1.00 17.38 DIC ATOM 999 CD2 LEU 131 28.981 61.583 73.722 1.00 15.49 DIC ATOM 1000 C LEU 131 25.168 58.428 73.974 1.00 11.77 DIC ATOM 1001 O LEU 131 24.367 58.755 74.853 1.00 10.73 DIC ATOM 1002 N PHE 132 24.789 58.045 72.760 1.00 11.04 DIC ATOM 1003 CA PHE 132 23.381 57.988 72.388 1.00 12.06 DIC ATOM 1004 CB PHE 132 23.244 57.642 70.903 1.00 14.10 DIC ATOM 1005 CG PHE 132 21.820 57.544 70.433 1.00 16.45 DIC ATOM 1006 CD1 PHE 132 21.121 56.346 70.531 1.00 16.62 DIC ATOM 1007 CD2 PHE 132 21.167 58.658 69.922 1.00 19.15 DIC ATOM 1008 CE1 PHE 132 19.793 56.257 70.128 1.00 16.52 DIC ATOM 1009 CE2 PHE 132 19.834 58.582 69.515 1.00 19.44 DIC ATOM 1010 CZ PHE 132 19.148 57.378 69.619 1.00 18.41 DIC ATOM 1011 C PHE 132 22.589 56.988 73.230 1.00 12.25 DIC ATOM 1012 O PHE 132 21.542 57.327 73.789 1.00 12.83 DIC ATOM 1013 N VAL 133 23.086 55.757 73.321 1.00 10.53 DIC ATOM 1014 CA VAL 133 22.404 54.722 74.093 1.00 10.89 DIC ATOM 1015 CB VAL 133 23.017 53.330 73.843 1.00 10.97 DIC ATOM 1016 CG1 VAL 133 22.268 52.280 74.669 1.00 12.18 DIC ATOM 1017 CG2 VAL 133 22.953 52.987 72.365 1.00 10.49 DIC ATOM 1018 C VAL 133 22.481 55.006 75.586 1.00 12.00 DIC ATOM 1019 O VAL 133 21.532 54.746 76.327 1.00 10.73 DIC ATOM 1020 N GLU 134 23.620 55.533 76.022 1.00 12.24 DIC ATOM 1021 CA GLU 134 23.822 55.843 77.431 1.00 14.14 DIC ATOM 1022 CB GLU 134 25.250 56.354 77.656 1.00 14.36 DIC ATOM 1023 CG GLU 134 25.592 56.614 79.114 1.00 16.20 DIC ATOM 1024 CD GLU 134 25.664 55.348 79.951 1.00 14.45 DIC ATOM 1025 OE1 GLU 134 25.645 55.468 81.189 1.00 17.32 DIC ATOM 1026 OE2 GLU 134 25.750 54.235 79.383 1.00 14.66 DIC ATOM 1027 C GLU 134 22.813 56.872 77.927 1.00 14.91 DIC ATOM 1028 O GLU 134 22.415 56.845 79.090 1.00 16.45 DIC ATOM 1029 N ARG 135 22.388 57.776 77.051 1.00 16.10 DIC ATOM 1030 CA ARG 135 21.428 58.792 77.454 1.00 16.53 DIC ATOM 1031 CB ARG 135 21.785 60.150 76.834 1.00 19.31 DIC ATOM 1032 CG ARG 135 21.548 60.279 75.341 1.00 22.07 DIC ATOM 1033 CD ARG 135 22.304 61.487 74.800 1.00 26.30 DIC ATOM 1034 NE ARG 135 21.972 62.716 75.516 1.00 29.13 DIC ATOM 1035 CZ ARG 135 20.851 63.410 75.339 1.00 32.01 DIC ATOM 1036 NH1 ARG 135 20.635 64.516 76.041 1.00 31.51 DIC ATOM 1037 NH2 ARG 135 19.950 63.007 74.450 1.00 32.01 DIC ATOM 1038 C ARG 135 19.992 58.405 77.110 1.00 17.25 DIC ATOM 1039 O ARG 135 19.078 59.217 77.232 1.00 17.38 DIC ATOM 1040 N GLN 136 19.800 57.164 76.674 1.00 15.73 DIC ATOM 1041 CA GLN 136 18.462 56.673 76.361 1.00 17.42 DIC ATOM 1042 CB GLN 136 18.538 55.479 75.413 1.00 16.78 DIC ATOM 1043 CG GLN 136 17.213 55.086 74.796 1.00 18.64 DIC ATOM 1044 CD GLN 136 17.355 53.916 73.845 1.00 21.61 DIC ATOM 1045 OE1 GLN 136 18.327 53.833 73.097 1.00 23.71 DIC ATOM 1046 NE2 GLN 136 16.383 53.012 73.861 1.00 21.40 DIC ATOM 1047 C GLN 136 17.905 56.236 77.713 1.00 18.33 DIC ATOM 1048 O GLN 136 18.123 55.106 78.149 1.00 16.98 DIC ATOM 1049 N GLU 137 17.199 57.146 78.375 1.00 20.02 DIC ATOM 1050 CA GLU 137 16.649 56.895 79.705 1.00 22.25 DIC ATOM 1051 CB GLU 137 15.653 58.004 80.072 1.00 26.10 DIC ATOM 1052 CG GLU 137 15.839 58.561 81.485 1.00 31.74 DIC ATOM 1053 CD GLU 137 15.083 57.774 82.544 1.00 35.77 DIC ATOM 1054 OE1 GLU 137 13.842 57.916 82.611 1.00 38.12 DIC ATOM 1055 OE2 GLU 137 15.723 57.016 83.308 1.00 36.14 DIC ATOM 1056 C GLU 137 16.008 55.529 79.927 1.00 20.26 DIC ATOM 1057 O GLU 137 15.064 55.145 79.234 1.00 21.74 DIC ATOM 1058 N GLY 138 16.547 54.798 80.898 1.00 19.39 DIC ATOM 1059 CA GLY 138 16.023 53.488 81.244 1.00 17.93 DIC ATOM 1060 C GLY 138 16.402 52.294 80.383 1.00 16.30 DIC ATOM 1061 O GLY 138 16.196 51.156 80.799 1.00 16.99 DIC ATOM 1062 N TYR 139 16.955 52.520 79.196 1.00 14.22 DIC ATOM 1063 CA TYR 139 17.303 51.392 78.340 1.00 12.95 DIC ATOM 1064 CB TYR 139 17.775 51.852 76.962 1.00 11.93 DIC ATOM 1065 CG TYR 139 18.077 50.670 76.066 1.00 9.65 DIC ATOM 1066 CD1 TYR 139 17.051 49.841 75.618 1.00 9.55 DIC ATOM 1067 CE1 TYR 139 17.318 48.699 74.870 1.00 6.57 DIC ATOM 1068 CD2 TYR 139 19.390 50.327 75.735 1.00 8.27 DIC ATOM 1069 CE2 TYR 139 19.668 49.180 74.983 1.00 6.71 DIC ATOM 1070 CZ TYR 139 18.622 48.372 74.558 1.00 6.55 DIC ATOM 1071 OH TYR 139 18.868 47.224 73.836 1.00 7.26 DIC ATOM 1072 C TYR 139 18.372 50.479 78.916 1.00 12.54 DIC ATOM 1073 O TYR 139 18.174 49.274 79.025 1.00 14.54 DIC ATOM 1074 N LYS 140 19.511 51.066 79.257 1.00 12.11 DIC ATOM 1075 CA LYS 140 20.643 50.335 79.801 1.00 12.14 DIC ATOM 1076 CB LYS 140 21.660 51.338 80.350 1.00 14.79 DIC ATOM 1077 CG LYS 140 22.981 50.743 80.761 1.00 17.75 DIC ATOM 1078 CD LYS 140 24.029 51.821 81.007 1.00 15.95 DIC ATOM 1079 CE LYS 140 23.711 52.669 82.224 1.00 17.64 DIC ATOM 1080 NZ LYS 140 24.887 53.502 82.602 1.00 16.20 DIC ATOM 1081 C LYS 140 20.229 49.344 80.884 1.00 13.45 DIC ATOM 1082 O LYS 140 20.690 48.201 80.903 1.00 13.33 DIC ATOM 1083 N GLN 141 19.348 49.776 81.778 1.00 11.99 DIC ATOM 1084 CA GLN 141 18.890 48.917 82.860 1.00 14.94 DIC ATOM 1085 CB GLN 141 18.150 49.752 83.914 1.00 15.97 DIC ATOM 1086 CG GLN 141 19.049 50.738 84.676 1.00 16.22 DIC ATOM 1087 CD GLN 141 19.452 51.962 83.859 1.00 19.15 DIC ATOM 1088 OE1 GLN 141 19.056 52.118 82.702 1.00 20.43 DIC ATOM 1089 NE2 GLN 141 20.240 52.843 84.469 1.00 16.02 DIC ATOM 1090 C GLN 141 18.008 47.766 82.369 1.00 14.90 DIC ATOM 1091 O GLN 141 17.990 46.686 82.968 1.00 15.34 DIC ATOM 1092 N LYS 142 17.284 47.992 81.278 1.00 14.30 DIC ATOM 1093 CA LYS 142 16.427 46.957 80.716 1.00 15.53 DIC ATOM 1094 CB LYS 142 15.698 47.475 79.470 1.00 17.58 DIC ATOM 1095 CG LYS 142 14.482 48.333 79.757 1.00 21.30 DIC ATOM 1096 CD LYS 142 13.895 48.879 78.459 1.00 25.10 DIC ATOM 1097 CE LYS 142 12.527 49.508 78.678 1.00 28.09 DIC ATOM 1098 NZ LYS 142 11.484 48.490 78.984 1.00 31.88 DIC ATOM 1099 C LYS 142 17.229 45.709 80.351 1.00 14.42 DIC ATOM 1100 O LYS 142 16.684 44.606 80.317 1.00 15.12 DIC ATOM 1101 N ILE 143 18.517 45.870 80.060 1.00 12.66 DIC ATOM 1102 CA ILE 143 19.319 44.699 79.724 1.00 11.78 DIC ATOM 1103 CB ILE 143 20.131 44.898 78.421 1.00 11.52 DIC ATOM 1104 CG2 ILE 143 19.177 45.095 77.249 1.00 9.94 DIC ATOM 1105 CG1 ILE 143 21.084 46.085 78.550 1.00 10.92 DIC ATOM 1106 CD ILE 143 22.037 46.202 77.376 1.00 9.97 DIC ATOM 1107 C ILE 143 20.246 44.268 80.863 1.00 11.61 DIC ATOM 1108 O ILE 143 21.264 43.612 80.639 1.00 11.97 DIC ATOM 1109 N GLY 144 19.873 44.649 82.085 1.00 11.10 DIC ATOM 1110 CA GLY 144 20.624 44.268 83.270 1.00 9.94 DIC ATOM 1111 C GLY 144 21.853 45.060 83.663 1.00 11.04 DIC ATOM 1112 O GLY 144 22.626 44.621 84.518 1.00 9.79 DIC ATOM 1113 N MSE 145 22.048 46.227 83.062 1.00 10.12 DIC ATOM 1114 CA MSE 145 23.212 47.031 83.390 1.00 11.90 DIC ATOM 1115 CB MSE 145 23.725 47.738 82.135 1.00 12.20 DIC ATOM 1116 CG MSE 145 24.329 46.789 81.111 1.00 13.32 DIC ATOM 1117 SE MSE 145 24.908 47.720 79.517 1.00 19.71 DIC ATOM 1118 CE MSE 145 26.468 48.596 80.243 1.00 14.79 DIC ATOM 1119 C MSE 145 22.931 48.048 84.487 1.00 12.83 DIC ATOM 1120 O MSE 145 21.821 48.576 84.594 1.00 11.70 DIC ATOM 1121 N ALA 146 23.948 48.314 85.301 1.00 14.28 DIC ATOM 1122 CA ALA 146 23.832 49.274 86.395 1.00 14.92 DIC ATOM 1123 CB ALA 146 24.793 48.903 87.517 1.00 14.61 DIC ATOM 1124 C ALA 146 24.140 50.677 85.891 1.00 15.53 DIC ATOM 1125 O ALA 146 24.776 50.843 84.852 1.00 14.24 DIC ATOM 1126 N ASP 147 23.688 51.683 86.634 1.00 16.07 DIC ATOM 1127 CA ASP 147 23.917 53.075 86.262 1.00 16.26 DIC ATOM 1128 CB ASP 147 23.370 54.011 87.346 1.00 20.59 DIC ATOM 1129 CG ASP 147 23.700 55.473 87.078 1.00 23.36 DIC ATOM 1130 OD1 ASP 147 23.214 56.026 86.069 1.00 25.96 DIC ATOM 1131 OD2 ASP 147 24.451 56.071 87.878 1.00 28.48 DIC ATOM 1132 C ASP 147 25.400 53.352 86.066 1.00 14.79 DIC ATOM 1133 O ASP 147 25.780 54.135 85.194 1.00 13.86 DIC ATOM 1134 N GLY 148 26.230 52.697 86.876 1.00 13.02 DIC ATOM 1135 CA GLY 148 27.668 52.894 86.806 1.00 11.35 DIC ATOM 1136 C GLY 148 28.396 52.094 85.744 1.00 10.20 DIC ATOM 1137 O GLY 148 29.606 52.246 85.574 1.00 11.09 DIC ATOM 1138 N GLU 149 27.676 51.225 85.043 1.00 9.04 DIC ATOM 1139 CA GLU 149 28.277 50.429 83.979 1.00 9.03 DIC ATOM 1140 CB GLU 149 27.733 49.001 84.003 1.00 8.78 DIC ATOM 1141 CG GLU 149 27.982 48.306 85.330 1.00 12.20 DIC ATOM 1142 CD GLU 149 27.390 46.916 85.382 1.00 11.83 DIC ATOM 1143 OE1 GLU 149 26.235 46.747 84.947 1.00 12.11 DIC ATOM 1144 OE2 GLU 149 28.073 45.994 85.871 1.00 16.06 DIC ATOM 1145 C GLU 149 27.884 51.142 82.697 1.00 8.47 DIC ATOM 1146 O GLU 149 26.701 51.294 82.393 1.00 9.02 DIC ATOM 1147 N TYR 150 28.886 51.591 81.956 1.00 8.23 DIC ATOM 1148 CA TYR 150 28.645 52.343 80.738 1.00 9.12 DIC ATOM 1149 CB TYR 150 29.760 53.383 80.590 1.00 8.51 DIC ATOM 1150 CG TYR 150 29.912 54.216 81.854 1.00 9.43 DIC ATOM 1151 CD1 TYR 150 31.155 54.388 82.461 1.00 10.16 DIC ATOM 1152 CE1 TYR 150 31.283 55.106 83.654 1.00 10.95 DIC ATOM 1153 CD2 TYR 150 28.796 54.790 82.469 1.00 12.27 DIC ATOM 1154 CE2 TYR 150 28.913 55.511 83.662 1.00 10.90 DIC ATOM 1155 CZ TYR 150 30.160 55.661 84.248 1.00 13.06 DIC ATOM 1156 OH TYR 150 30.279 56.354 85.433 1.00 12.48 DIC ATOM 1157 C TYR 150 28.488 51.494 79.487 1.00 7.57 DIC ATOM 1158 O TYR 150 29.309 50.625 79.187 1.00 6.61 DIC ATOM 1159 N TYR 151 27.401 51.755 78.769 1.00 7.71 DIC ATOM 1160 CA TYR 151 27.069 51.035 77.547 1.00 7.79 DIC ATOM 1161 CB TYR 151 25.629 51.375 77.144 1.00 6.89 DIC ATOM 1162 CG TYR 151 25.057 50.553 76.009 1.00 7.54 DIC ATOM 1163 CD1 TYR 151 25.432 50.789 74.685 1.00 5.74 DIC ATOM 1164 CE1 TYR 151 24.889 50.039 73.635 1.00 4.54 DIC ATOM 1165 CD2 TYR 151 24.125 49.546 76.260 1.00 7.45 DIC ATOM 1166 CE2 TYR 151 23.579 48.792 75.222 1.00 6.69 DIC ATOM 1167 CZ TYR 151 23.964 49.042 73.913 1.00 6.52 DIC ATOM 1168 OH TYR 151 23.432 48.282 72.891 1.00 6.05 DIC ATOM 1169 C TYR 151 28.047 51.443 76.454 1.00 6.36 DIC ATOM 1170 O TYR 151 28.148 52.621 76.116 1.00 7.50 DIC ATOM 1171 N PHE 152 28.776 50.475 75.909 1.00 5.53 DIC ATOM 1172 CA PHE 152 29.745 50.779 74.870 1.00 4.94 DIC ATOM 1173 CB PHE 152 31.060 50.016 75.108 1.00 4.86 DIC ATOM 1174 CG PHE 152 30.919 48.513 75.089 1.00 6.40 DIC ATOM 1175 CD1 PHE 152 30.724 47.802 76.271 1.00 6.43 DIC ATOM 1176 CD2 PHE 152 30.984 47.808 73.888 1.00 4.17 DIC ATOM 1177 CE1 PHE 152 30.594 46.408 76.259 1.00 5.71 DIC ATOM 1178 CE2 PHE 152 30.854 46.416 73.865 1.00 5.71 DIC ATOM 1179 CZ PHE 152 30.659 45.717 75.055 1.00 5.50 DIC ATOM 1180 C PHE 152 29.229 50.481 73.470 1.00 5.82 DIC ATOM 1181 O PHE 152 28.301 49.695 73.290 1.00 5.93 DIC ATOM 1182 N ASN 153 29.828 51.133 72.481 1.00 5.20 DIC ATOM 1183 CA ASN 153 29.447 50.910 71.094 1.00 5.79 DIC ATOM 1184 CB ASN 153 29.685 52.176 70.260 1.00 6.58 DIC ATOM 1185 CG ASN 153 29.282 51.998 68.809 1.00 6.46 DIC ATOM 1186 OD1 ASN 153 30.095 51.621 67.974 1.00 6.69 DIC ATOM 1187 ND2 ASN 153 28.011 52.247 68.510 1.00 9.09 DIC ATOM 1188 C ASN 153 30.296 49.752 70.585 1.00 5.25 DIC ATOM 1189 O ASN 153 31.492 49.683 70.861 1.00 3.87 DIC ATOM 1190 N ALA 154 29.674 48.838 69.847 1.00 5.40 DIC ATOM 1191 CA ALA 154 30.373 47.661 69.336 1.00 7.13 DIC ATOM 1192 CB ALA 154 29.381 46.508 69.188 1.00 4.44 DIC ATOM 1193 C ALA 154 31.134 47.859 68.024 1.00 6.42 DIC ATOM 1194 O ALA 154 31.733 46.913 67.507 1.00 7.14 DIC ATOM 1195 N GLY 155 31.118 49.080 67.496 1.00 6.03 DIC ATOM 1196 CA GLY 155 31.792 49.359 66.239 1.00 4.30 DIC ATOM 1197 C GLY 155 33.312 49.368 66.250 1.00 6.06 DIC ATOM 1198 O GLY 155 33.939 49.273 65.192 1.00 4.92 DIC ATOM 1199 N VAL 156 33.907 49.496 67.433 1.00 4.75 DIC ATOM 1200 CA VAL 156 35.362 49.510 67.582 1.00 4.31 DIC ATOM 1201 CB VAL 156 35.901 50.954 67.701 1.00 5.59 DIC ATOM 1202 CG1 VAL 156 37.398 50.931 67.984 1.00 5.38 DIC ATOM 1203 CG2 VAL 156 35.617 51.727 66.405 1.00 2.76 DIC ATOM 1204 C VAL 156 35.686 48.741 68.855 1.00 5.47 DIC ATOM 1205 O VAL 156 35.396 49.203 69.959 1.00 5.04 DIC ATOM 1206 N LEU 157 36.300 47.573 68.703 1.00 4.91 DIC ATOM 1207 CA LEU 157 36.599 46.741 69.858 1.00 6.02 DIC ATOM 1208 CB LEU 157 35.606 45.580 69.908 1.00 5.28 DIC ATOM 1209 CG LEU 157 34.120 45.923 69.800 1.00 5.55 DIC ATOM 1210 CD1 LEU 157 33.324 44.655 69.516 1.00 3.12 DIC ATOM 1211 CD2 LEU 157 33.658 46.599 71.084 1.00 3.69 DIC ATOM 1212 C LEU 157 37.998 46.157 69.915 1.00 6.93 DIC ATOM 1213 O LEU 157 38.403 45.431 69.008 1.00 7.95 DIC ATOM 1214 N LEU 158 38.733 46.474 70.978 1.00 6.51 DIC ATOM 1215 CA LEU 158 40.059 45.897 71.174 1.00 6.78 DIC ATOM 1216 CB LEU 158 40.956 46.826 71.995 1.00 8.24 DIC ATOM 1217 CG LEU 158 42.416 46.378 72.110 1.00 8.34 DIC ATOM 1218 CD1 LEU 158 43.062 46.337 70.728 1.00 8.63 DIC ATOM 1219 CD2 LEU 158 43.164 47.331 73.018 1.00 9.77 DIC ATOM 1220 C LEU 158 39.693 44.652 71.978 1.00 7.75 DIC ATOM 1221 O LEU 158 39.304 44.740 73.146 1.00 5.84 DIC ATOM 1222 N ILE 159 39.803 43.493 71.343 1.00 7.13 DIC ATOM 1223 CA ILE 159 39.401 42.246 71.973 1.00 7.06 DIC ATOM 1224 CB ILE 159 38.582 41.418 70.951 1.00 8.06 DIC ATOM 1225 CG2 ILE 159 38.329 40.009 71.467 1.00 5.92 DIC ATOM 1226 CG1 ILE 159 37.274 42.160 70.652 1.00 7.50 DIC ATOM 1227 CD ILE 159 36.439 41.533 69.576 1.00 12.31 DIC ATOM 1228 C ILE 159 40.494 41.377 72.585 1.00 8.00 DIC ATOM 1229 O ILE 159 41.513 41.099 71.958 1.00 5.43 DIC ATOM 1230 N ASN 160 40.261 40.952 73.824 1.00 8.08 DIC ATOM 1231 CA ASN 160 41.198 40.079 74.530 1.00 8.60 DIC ATOM 1232 CB ASN 160 40.987 40.197 76.037 1.00 9.75 DIC ATOM 1233 CG ASN 160 41.948 39.334 76.838 1.00 8.59 DIC ATOM 1234 OD1 ASN 160 42.542 38.393 76.317 1.00 6.73 DIC ATOM 1235 ND2 ASN 160 42.092 39.648 78.119 1.00 8.57 DIC ATOM 1236 C ASN 160 40.857 38.665 74.066 1.00 9.81 DIC ATOM 1237 O ASN 160 40.217 37.898 74.793 1.00 9.36 DIC ATOM 1238 N LEU 161 41.276 38.331 72.849 1.00 11.11 DIC ATOM 1239 CA LEU 161 40.987 37.024 72.268 1.00 11.84 DIC ATOM 1240 CB LEU 161 41.603 36.905 70.871 1.00 13.69 DIC ATOM 1241 CG LEU 161 40.670 37.132 69.680 1.00 18.63 DIC ATOM 1242 CD1 LEU 161 41.441 36.900 68.392 1.00 17.69 DIC ATOM 1243 CD2 LEU 161 39.479 36.185 69.753 1.00 17.40 DIC ATOM 1244 C LEU 161 41.423 35.830 73.104 1.00 12.22 DIC ATOM 1245 O LEU 161 40.733 34.811 73.132 1.00 10.35 DIC ATOM 1246 N LYS 162 42.568 35.935 73.769 1.00 12.29 DIC ATOM 1247 CA LYS 162 43.031 34.823 74.591 1.00 13.27 DIC ATOM 1248 CB LYS 162 44.369 35.159 75.261 1.00 16.11 DIC ATOM 1249 CG LYS 162 44.829 34.102 76.258 1.00 20.91 DIC ATOM 1250 CD LYS 162 46.278 34.286 76.686 1.00 24.43 DIC ATOM 1251 CE LYS 162 47.247 33.739 75.643 1.00 27.26 DIC ATOM 1252 NZ LYS 162 48.647 33.711 76.161 1.00 27.23 DIC ATOM 1253 C LYS 162 41.975 34.491 75.643 1.00 12.71 DIC ATOM 1254 O LYS 162 41.677 33.325 75.878 1.00 13.95 DIC ATOM 1255 N LYS 163 41.400 35.516 76.268 1.00 12.30 DIC ATOM 1256 CA LYS 163 40.369 35.287 77.275 1.00 10.73 DIC ATOM 1257 CB LYS 163 40.006 36.594 77.987 1.00 9.94 DIC ATOM 1258 CG LYS 163 38.984 36.419 79.113 1.00 9.80 DIC ATOM 1259 CD LYS 163 38.667 37.744 79.792 1.00 12.02 DIC ATOM 1260 CE LYS 163 37.685 37.563 80.946 1.00 11.59 DIC ATOM 1261 NZ LYS 163 38.230 36.656 81.994 1.00 15.21 DIC ATOM 1262 C LYS 163 39.120 34.695 76.616 1.00 10.32 DIC ATOM 1263 O LYS 163 38.527 33.748 77.133 1.00 10.04 DIC ATOM 1264 N TRP 164 38.718 35.260 75.481 1.00 10.10 DIC ATOM 1265 CA TRP 164 37.545 34.768 74.762 1.00 10.66 DIC ATOM 1266 CB TRP 164 37.366 35.524 73.443 1.00 8.99 DIC ATOM 1267 CG TRP 164 36.729 36.883 73.567 1.00 7.04 DIC ATOM 1268 CD2 TRP 164 35.780 37.469 72.665 1.00 6.04 DIC ATOM 1269 CE2 TRP 164 35.516 38.777 73.127 1.00 5.54 DIC ATOM 1270 CE3 TRP 164 35.131 37.015 71.508 1.00 5.98 DIC ATOM 1271 CD1 TRP 164 36.989 37.829 74.514 1.00 7.19 DIC ATOM 1272 NE1 TRP 164 36.265 38.970 74.257 1.00 6.74 DIC ATOM 1273 CZ2 TRP 164 34.630 39.642 72.471 1.00 7.14 DIC ATOM 1274 CZ3 TRP 164 34.249 37.873 70.856 1.00 6.29 DIC ATOM 1275 CH2 TRP 164 34.008 39.174 71.342 1.00 6.21 DIC ATOM 1276 C TRP 164 37.657 33.271 74.464 1.00 11.95 DIC ATOM 1277 O TRP 164 36.695 32.519 74.642 1.00 9.24 DIC ATOM 1278 N ARG 165 38.829 32.841 74.005 1.00 11.53 DIC ATOM 1279 CA ARG 165 39.025 31.433 73.677 1.00 12.97 DIC ATOM 1280 CB ARG 165 40.392 31.220 73.011 1.00 13.33 DIC ATOM 1281 CG ARG 165 40.431 31.666 71.546 1.00 16.11 DIC ATOM 1282 CD ARG 165 41.607 31.041 70.792 1.00 16.25 DIC ATOM 1283 NE ARG 165 42.889 31.519 71.293 1.00 16.10 DIC ATOM 1284 CZ ARG 165 43.467 32.653 70.914 1.00 16.79 DIC ATOM 1285 NH1 ARG 165 44.632 33.005 71.440 1.00 19.33 DIC ATOM 1286 NH2 ARG 165 42.898 33.423 69.994 1.00 15.46 DIC ATOM 1287 C ARG 165 38.858 30.495 74.871 1.00 13.30 DIC ATOM 1288 O ARG 165 38.699 29.292 74.698 1.00 13.71 DIC ATOM 1289 N ARG 166 38.876 31.041 76.081 1.00 14.72 DIC ATOM 1290 CA ARG 166 38.699 30.218 77.277 1.00 14.91 DIC ATOM 1291 CB ARG 166 39.333 30.891 78.497 1.00 16.73 DIC ATOM 1292 CG ARG 166 40.852 30.924 78.497 1.00 18.26 DIC ATOM 1293 CD ARG 166 41.361 31.920 79.529 1.00 19.78 DIC ATOM 1294 NE ARG 166 42.817 32.015 79.525 1.00 23.68 DIC ATOM 1295 CZ ARG 166 43.494 33.142 79.725 1.00 22.99 DIC ATOM 1296 NH1 ARG 166 42.847 34.279 79.943 1.00 23.36 DIC ATOM 1297 NH2 ARG 166 44.820 33.133 79.697 1.00 25.53 DIC ATOM 1298 C ARG 166 37.213 29.999 77.558 1.00 14.47 DIC ATOM 1299 O ARG 166 36.854 29.254 78.463 1.00 14.64 DIC ATOM 1300 N HIS 167 36.352 30.640 76.776 1.00 13.19 DIC ATOM 1301 CA HIS 167 34.912 30.523 76.990 1.00 13.58 DIC ATOM 1302 CB HIS 167 34.380 31.815 77.624 1.00 14.56 DIC ATOM 1303 CG HIS 167 35.031 32.166 78.928 1.00 15.72 DIC ATOM 1304 CD2 HIS 167 36.121 32.920 79.206 1.00 14.81 DIC ATOM 1305 ND1 HIS 167 34.570 31.700 80.141 1.00 15.43 DIC ATOM 1306 CE1 HIS 167 35.347 32.151 81.109 1.00 14.64 DIC ATOM 1307 NE2 HIS 167 36.296 32.895 80.568 1.00 15.87 DIC ATOM 1308 C HIS 167 34.145 30.251 75.701 1.00 13.20 DIC ATOM 1309 O HIS 167 34.673 30.410 74.600 1.00 14.22 DIC ATOM 1310 N ASP 168 32.894 29.831 75.848 1.00 10.69 DIC ATOM 1311 CA ASP 168 32.045 29.572 74.699 1.00 10.18 DIC ATOM 1312 CB ASP 168 31.212 28.303 74.914 1.00 11.40 DIC ATOM 1313 CG ASP 168 30.499 27.860 73.654 1.00 11.10 DIC ATOM 1314 OD1 ASP 168 30.114 26.676 73.566 1.00 13.98 DIC ATOM 1315 OD2 ASP 168 30.317 28.698 72.748 1.00 13.04 DIC ATOM 1316 C ASP 168 31.150 30.801 74.568 1.00 9.57 DIC ATOM 1317 O ASP 168 30.019 30.830 75.056 1.00 6.68 DIC ATOM 1318 N ILE 169 31.690 31.818 73.904 1.00 8.34 DIC ATOM 1319 CA ILE 169 31.001 33.084 73.710 1.00 8.76 DIC ATOM 1320 CB ILE 169 31.918 34.092 72.985 1.00 8.29 DIC ATOM 1321 CG2 ILE 169 31.221 35.441 72.863 1.00 8.00 DIC ATOM 1322 CG1 ILE 169 33.230 34.244 73.759 1.00 10.02 DIC ATOM 1323 CD ILE 169 33.046 34.721 75.202 1.00 11.51 DIC ATOM 1324 C ILE 169 29.689 32.963 72.947 1.00 7.31 DIC ATOM 1325 O ILE 169 28.718 33.644 73.270 1.00 7.10 DIC ATOM 1326 N PHE 170 29.653 32.102 71.937 1.00 9.62 DIC ATOM 1327 CA PHE 170 28.428 31.936 71.162 1.00 9.67 DIC ATOM 1328 CB PHE 170 28.670 31.053 69.941 1.00 11.96 DIC ATOM 1329 CG PHE 170 27.451 30.875 69.082 1.00 12.14 DIC ATOM 1330 CD1 PHE 170 26.782 29.657 69.043 1.00 15.39 DIC ATOM 1331 CD2 PHE 170 26.950 31.939 68.339 1.00 13.78 DIC ATOM 1332 CE1 PHE 170 25.628 29.500 68.276 1.00 16.66 DIC ATOM 1333 CE2 PHE 170 25.800 31.793 67.569 1.00 16.17 DIC ATOM 1334 CZ PHE 170 25.136 30.569 67.539 1.00 15.75 DIC ATOM 1335 C PHE 170 27.314 31.336 72.012 1.00 10.61 DIC ATOM 1336 O PHE 170 26.163 31.765 71.933 1.00 10.59 DIC ATOM 1337 N LYS 171 27.652 30.345 72.830 1.00 10.05 DIC ATOM 1338 CA LYS 171 26.648 29.723 73.682 1.00 10.03 DIC ATOM 1339 CB LYS 171 27.239 28.505 74.399 1.00 13.97 DIC ATOM 1340 CG LYS 171 26.201 27.670 75.138 1.00 18.06 DIC ATOM 1341 CD LYS 171 26.735 26.285 75.464 1.00 22.03 DIC ATOM 1342 CE LYS 171 27.078 25.516 74.194 1.00 24.58 DIC ATOM 1343 NZ LYS 171 27.566 24.142 74.489 1.00 29.13 DIC ATOM 1344 C LYS 171 26.137 30.743 74.699 1.00 9.12 DIC ATOM 1345 O LYS 171 24.935 30.853 74.928 1.00 9.26 DIC ATOM 1346 N MSE 172 27.058 31.485 75.303 1.00 6.97 DIC ATOM 1347 CA MSE 172 26.708 32.512 76.278 1.00 9.01 DIC ATOM 1348 CB MSE 172 27.980 33.168 76.828 1.00 11.24 DIC ATOM 1349 CG MSE 172 28.846 32.238 77.665 1.00 13.80 DIC ATOM 1350 SE MSE 172 30.625 32.946 77.970 1.00 25.22 DIC ATOM 1351 CE MSE 172 30.177 34.354 79.221 1.00 18.63 DIC ATOM 1352 C MSE 172 25.836 33.562 75.593 1.00 9.14 DIC ATOM 1353 O MSE 172 24.924 34.123 76.202 1.00 10.30 DIC ATOM 1354 N SER 173 26.126 33.819 74.320 1.00 7.61 DIC ATOM 1355 CA SER 173 25.364 34.790 73.543 1.00 8.52 DIC ATOM 1356 CB SER 173 26.038 35.042 72.191 1.00 8.17 DIC ATOM 1357 OG SER 173 27.276 35.717 72.350 1.00 7.46 DIC ATOM 1358 C SER 173 23.945 34.278 73.316 1.00 9.07 DIC ATOM 1359 O SER 173 22.972 35.020 73.482 1.00 7.42 DIC ATOM 1360 N SER 174 23.837 33.008 72.935 1.00 7.76 DIC ATOM 1361 CA SER 174 22.539 32.397 72.682 1.00 9.45 DIC ATOM 1362 CB SER 174 22.718 30.952 72.210 1.00 9.22 DIC ATOM 1363 OG SER 174 23.382 30.917 70.961 1.00 8.11 DIC ATOM 1364 C SER 174 21.651 32.428 73.916 1.00 9.49 DIC ATOM 1365 O SER 174 20.460 32.725 73.824 1.00 9.51 DIC ATOM 1366 N GLU 175 22.234 32.123 75.071 1.00 10.06 DIC ATOM 1367 CA GLU 175 21.486 32.118 76.321 1.00 11.19 DIC ATOM 1368 CB GLU 175 22.336 31.537 77.452 1.00 14.11 DIC ATOM 1369 CG GLU 175 22.905 30.162 77.158 1.00 18.91 DIC ATOM 1370 CD GLU 175 23.568 29.540 78.372 1.00 21.75 DIC ATOM 1371 OE1 GLU 175 24.311 30.255 79.079 1.00 21.00 DIC ATOM 1372 OE2 GLU 175 23.350 28.333 78.615 1.00 24.48 DIC ATOM 1373 C GLU 175 21.046 33.525 76.697 1.00 10.40 DIC ATOM 1374 O GLU 175 19.942 33.725 77.202 1.00 10.43 DIC ATOM 1375 N TRP 176 21.912 34.502 76.453 1.00 11.21 DIC ATOM 1376 CA TRP 176 21.588 35.886 76.778 1.00 10.92 DIC ATOM 1377 CB TRP 176 22.804 36.788 76.550 1.00 11.86 DIC ATOM 1378 CG TRP 176 22.661 38.151 77.172 1.00 10.34 DIC ATOM 1379 CD2 TRP 176 22.094 39.317 76.564 1.00 10.13 DIC ATOM 1380 CE2 TRP 176 22.131 40.350 77.525 1.00 10.66 DIC ATOM 1381 CE3 TRP 176 21.555 39.588 75.299 1.00 11.84 DIC ATOM 1382 CD1 TRP 176 23.009 38.513 78.440 1.00 10.51 DIC ATOM 1383 NE1 TRP 176 22.695 39.832 78.662 1.00 11.39 DIC ATOM 1384 CZ2 TRP 176 21.649 41.636 77.263 1.00 10.57 DIC ATOM 1385 CZ3 TRP 176 21.073 40.869 75.037 1.00 9.09 DIC ATOM 1386 CH2 TRP 176 21.124 41.876 76.016 1.00 10.83 DIC ATOM 1387 C TRP 176 20.422 36.351 75.903 1.00 10.57 DIC ATOM 1388 O TRP 176 19.496 37.008 76.386 1.00 10.92 DIC ATOM 1389 N VAL 177 20.474 36.008 74.617 1.00 9.67 DIC ATOM 1390 CA VAL 177 19.415 36.382 73.681 1.00 8.71 DIC ATOM 1391 CB VAL 177 19.737 35.905 72.245 1.00 10.47 DIC ATOM 1392 CG1 VAL 177 18.483 35.975 71.369 1.00 9.48 DIC ATOM 1393 CG2 VAL 177 20.836 36.771 71.642 1.00 5.59 DIC ATOM 1394 C VAL 177 18.091 35.758 74.118 1.00 10.57 DIC ATOM 1395 O VAL 177 17.027 36.376 74.019 1.00 9.35 DIC ATOM 1396 N GLU 178 18.160 34.524 74.597 1.00 11.52 DIC ATOM 1397 CA GLU 178 16.961 33.833 75.038 1.00 15.37 DIC ATOM 1398 CB GLU 178 17.310 32.407 75.471 1.00 16.80 DIC ATOM 1399 CG GLU 178 16.111 31.557 75.857 1.00 22.43 DIC ATOM 1400 CD GLU 178 15.023 31.554 74.797 1.00 25.01 DIC ATOM 1401 OE1 GLU 178 15.345 31.366 73.603 1.00 27.14 DIC ATOM 1402 OE2 GLU 178 13.841 31.735 75.161 1.00 29.11 DIC ATOM 1403 C GLU 178 16.355 34.603 76.204 1.00 15.38 DIC ATOM 1404 O GLU 178 15.139 34.679 76.352 1.00 15.87 DIC ATOM 1405 N GLN 179 17.223 35.198 77.012 1.00 15.89 DIC ATOM 1406 CA GLN 179 16.803 35.954 78.180 1.00 17.35 DIC ATOM 1407 CB GLN 179 17.962 35.998 79.182 1.00 19.05 DIC ATOM 1408 CG GLN 179 17.658 36.694 80.493 1.00 24.86 DIC ATOM 1409 CD GLN 179 18.839 36.659 81.454 1.00 27.98 DIC ATOM 1410 OE1 GLN 179 18.761 37.170 82.573 1.00 31.11 DIC ATOM 1411 NE2 GLN 179 19.939 36.053 81.019 1.00 29.53 DIC ATOM 1412 C GLN 179 16.313 37.375 77.884 1.00 16.67 DIC ATOM 1413 O GLN 179 15.381 37.850 78.528 1.00 17.16 DIC ATOM 1414 N TYR 180 16.918 38.045 76.904 1.00 15.88 DIC ATOM 1415 CA TYR 180 16.543 39.423 76.585 1.00 14.53 DIC ATOM 1416 CB TYR 180 17.736 40.347 76.831 1.00 15.01 DIC ATOM 1417 CG TYR 180 18.196 40.402 78.264 1.00 12.97 DIC ATOM 1418 CD1 TYR 180 19.108 39.476 78.765 1.00 13.79 DIC ATOM 1419 CE1 TYR 180 19.545 39.543 80.085 1.00 15.48 DIC ATOM 1420 CD2 TYR 180 17.725 41.393 79.121 1.00 14.79 DIC ATOM 1421 CE2 TYR 180 18.152 41.466 80.439 1.00 15.22 DIC ATOM 1422 CZ TYR 180 19.062 40.542 80.915 1.00 14.58 DIC ATOM 1423 OH TYR 180 19.489 40.624 82.222 1.00 18.45 DIC ATOM 1424 C TYR 180 16.011 39.696 75.177 1.00 15.69 DIC ATOM 1425 O TYR 180 15.974 40.846 74.741 1.00 14.37 DIC ATOM 1426 N LYS 181 15.597 38.650 74.474 1.00 15.60 DIC ATOM 1427 CA LYS 181 15.082 38.788 73.116 1.00 18.04 DIC ATOM 1428 CB LYS 181 14.660 37.415 72.585 1.00 19.59 DIC ATOM 1429 CG LYS 181 13.984 37.447 71.226 1.00 24.70 DIC ATOM 1430 CD LYS 181 14.910 37.984 70.145 1.00 27.36 DIC ATOM 1431 CE LYS 181 14.215 37.989 68.789 1.00 27.65 DIC ATOM 1432 NZ LYS 181 13.752 36.628 68.397 1.00 29.00 DIC ATOM 1433 C LYS 181 13.910 39.762 72.973 1.00 16.82 DIC ATOM 1434 O LYS 181 13.759 40.414 71.939 1.00 16.53 DIC ATOM 1435 N ASP 182 13.083 39.860 74.006 1.00 16.61 DIC ATOM 1436 CA ASP 182 11.915 40.738 73.964 1.00 18.34 DIC ATOM 1437 CB ASP 182 10.842 40.220 74.920 1.00 19.12 DIC ATOM 1438 CG ASP 182 10.268 38.885 74.492 1.00 20.80 DIC ATOM 1439 OD1 ASP 182 9.625 38.232 75.336 1.00 23.00 DIC ATOM 1440 OD2 ASP 182 10.447 38.491 73.317 1.00 23.17 DIC ATOM 1441 C ASP 182 12.197 42.199 74.301 1.00 17.72 DIC ATOM 1442 O ASP 182 11.312 43.042 74.178 1.00 19.56 DIC ATOM 1443 N VAL 183 13.416 42.507 74.724 1.00 16.43 DIC ATOM 1444 CA VAL 183 13.737 43.880 75.092 1.00 15.35 DIC ATOM 1445 CB VAL 183 14.003 43.979 76.619 1.00 17.44 DIC ATOM 1446 CG1 VAL 183 15.207 43.133 76.998 1.00 17.05 DIC ATOM 1447 CG2 VAL 183 14.215 45.422 77.022 1.00 21.13 DIC ATOM 1448 C VAL 183 14.914 44.489 74.334 1.00 14.50 DIC ATOM 1449 O VAL 183 14.957 45.703 74.122 1.00 13.37 DIC ATOM 1450 N MSE 184 15.863 43.659 73.914 1.00 13.04 DIC ATOM 1451 CA MSE 184 17.024 44.177 73.203 1.00 12.36 DIC ATOM 1452 CB MSE 184 18.002 43.038 72.852 1.00 15.98 DIC ATOM 1453 CG MSE 184 17.427 41.874 72.058 1.00 17.28 DIC ATOM 1454 SE MSE 184 18.615 40.314 72.140 1.00 23.65 DIC ATOM 1455 CE MSE 184 19.958 40.898 70.874 1.00 16.42 DIC ATOM 1456 C MSE 184 16.641 44.976 71.960 1.00 11.92 DIC ATOM 1457 O MSE 184 15.749 44.594 71.198 1.00 11.41 DIC ATOM 1458 N GLN 185 17.324 46.098 71.772 1.00 10.32 DIC ATOM 1459 CA GLN 185 17.066 46.983 70.647 1.00 10.61 DIC ATOM 1460 CB GLN 185 16.644 48.362 71.164 1.00 13.31 DIC ATOM 1461 CG GLN 185 15.271 48.406 71.823 1.00 13.72 DIC ATOM 1462 CD GLN 185 14.959 49.766 72.438 1.00 16.61 DIC ATOM 1463 OE1 GLN 185 15.407 50.805 71.944 1.00 14.88 DIC ATOM 1464 NE2 GLN 185 14.174 49.764 73.513 1.00 14.58 DIC ATOM 1465 C GLN 185 18.287 47.141 69.748 1.00 9.38 DIC ATOM 1466 O GLN 185 18.167 47.581 68.602 1.00 7.58 DIC ATOM 1467 N TYR 186 19.460 46.772 70.254 1.00 7.31 DIC ATOM 1468 CA TYR 186 20.670 46.938 69.465 1.00 8.32 DIC ATOM 1469 CB TYR 186 21.601 47.929 70.169 1.00 8.66 DIC ATOM 1470 CG TYR 186 20.939 49.274 70.383 1.00 12.08 DIC ATOM 1471 CD1 TYR 186 20.325 49.589 71.594 1.00 11.99 DIC ATOM 1472 CE1 TYR 186 19.659 50.805 71.774 1.00 11.92 DIC ATOM 1473 CD2 TYR 186 20.873 50.213 69.348 1.00 14.31 DIC ATOM 1474 CE2 TYR 186 20.210 51.428 69.516 1.00 13.76 DIC ATOM 1475 CZ TYR 186 19.605 51.716 70.732 1.00 13.90 DIC ATOM 1476 OH TYR 186 18.947 52.915 70.901 1.00 12.39 DIC ATOM 1477 C TYR 186 21.422 45.672 69.065 1.00 6.28 DIC ATOM 1478 O TYR 186 22.640 45.679 68.913 1.00 5.43 DIC ATOM 1479 N GLN 187 20.676 44.587 68.907 1.00 5.24 DIC ATOM 1480 CA GLN 187 21.217 43.316 68.445 1.00 5.09 DIC ATOM 1481 CB GLN 187 21.306 43.393 66.913 1.00 6.13 DIC ATOM 1482 CG GLN 187 20.085 44.111 66.309 1.00 6.96 DIC ATOM 1483 CD GLN 187 20.155 44.327 64.800 1.00 9.84 DIC ATOM 1484 OE1 GLN 187 21.221 44.577 64.235 1.00 11.83 DIC ATOM 1485 NE2 GLN 187 19.005 44.262 64.150 1.00 8.23 DIC ATOM 1486 C GLN 187 22.550 42.857 69.065 1.00 4.73 DIC ATOM 1487 O GLN 187 22.659 42.726 70.285 1.00 5.09 DIC ATOM 1488 N ASP 188 23.561 42.608 68.235 1.00 4.04 DIC ATOM 1489 CA ASP 188 24.849 42.128 68.740 1.00 4.79 DIC ATOM 1490 CB ASP 188 25.832 41.901 67.589 1.00 5.88 DIC ATOM 1491 CG ASP 188 26.115 43.164 66.807 1.00 7.65 DIC ATOM 1492 OD1 ASP 188 25.242 43.574 66.013 1.00 8.96 DIC ATOM 1493 OD2 ASP 188 27.203 43.747 66.990 1.00 5.04 DIC ATOM 1494 C ASP 188 25.493 43.049 69.770 1.00 4.86 DIC ATOM 1495 O ASP 188 26.208 42.595 70.671 1.00 3.28 DIC ATOM 1496 N GLN 189 25.236 44.342 69.633 1.00 4.17 DIC ATOM 1497 CA GLN 189 25.789 45.334 70.547 1.00 5.49 DIC ATOM 1498 CB GLN 189 25.421 46.730 70.050 1.00 4.71 DIC ATOM 1499 CG GLN 189 26.008 47.868 70.848 1.00 5.10 DIC ATOM 1500 CD GLN 189 25.851 49.189 70.117 1.00 6.21 DIC ATOM 1501 OE1 GLN 189 26.760 49.634 69.414 1.00 6.99 DIC ATOM 1502 NE2 GLN 189 24.684 49.809 70.258 1.00 5.59 DIC ATOM 1503 C GLN 189 25.258 45.101 71.963 1.00 5.73 DIC ATOM 1504 O GLN 189 25.990 45.232 72.940 1.00 5.04 DIC ATOM 1505 N ASP 190 23.980 44.755 72.064 1.00 6.60 DIC ATOM 1506 CA ASP 190 23.371 44.480 73.361 1.00 6.99 DIC ATOM 1507 CB ASP 190 21.873 44.203 73.200 1.00 6.82 DIC ATOM 1508 CG ASP 190 21.061 45.466 72.999 1.00 7.01 DIC ATOM 1509 OD1 ASP 190 19.957 45.369 72.422 1.00 5.87 DIC ATOM 1510 OD2 ASP 190 21.515 46.547 73.428 1.00 5.97 DIC ATOM 1511 C ASP 190 24.040 43.256 73.976 1.00 6.81 DIC ATOM 1512 O ASP 190 24.454 43.277 75.135 1.00 8.46 DIC ATOM 1513 N ILE 191 24.135 42.188 73.187 1.00 6.27 DIC ATOM 1514 CA ILE 191 24.747 40.947 73.645 1.00 5.03 DIC ATOM 1515 CB ILE 191 24.896 39.932 72.487 1.00 3.31 DIC ATOM 1516 CG2 ILE 191 25.566 38.655 72.999 1.00 1.40 DIC ATOM 1517 CG1 ILE 191 23.518 39.598 71.909 1.00 4.10 DIC ATOM 1518 CD ILE 191 23.555 38.693 70.687 1.00 1.67 DIC ATOM 1519 C ILE 191 26.118 41.188 74.259 1.00 5.12 DIC ATOM 1520 O ILE 191 26.389 40.751 75.376 1.00 6.29 DIC ATOM 1521 N LEU 192 26.979 41.890 73.529 1.00 4.92 DIC ATOM 1522 CA LEU 192 28.326 42.168 74.009 1.00 5.86 DIC ATOM 1523 CB LEU 192 29.107 42.956 72.955 1.00 6.75 DIC ATOM 1524 CG LEU 192 29.278 42.257 71.601 1.00 6.62 DIC ATOM 1525 CD1 LEU 192 29.967 43.202 70.626 1.00 6.82 DIC ATOM 1526 CD2 LEU 192 30.086 40.988 71.771 1.00 8.14 DIC ATOM 1527 C LEU 192 28.306 42.930 75.332 1.00 6.87 DIC ATOM 1528 O LEU 192 29.053 42.603 76.253 1.00 6.68 DIC ATOM 1529 N ASN 193 27.449 43.943 75.424 1.00 6.22 DIC ATOM 1530 CA ASN 193 27.339 44.732 76.650 1.00 8.19 DIC ATOM 1531 CB ASN 193 26.403 45.921 76.434 1.00 8.71 DIC ATOM 1532 CG ASN 193 27.139 47.159 75.972 1.00 9.44 DIC ATOM 1533 OD1 ASN 193 27.826 47.814 76.760 1.00 7.46 DIC ATOM 1534 ND2 ASN 193 27.007 47.487 74.690 1.00 6.34 DIC ATOM 1535 C ASN 193 26.827 43.897 77.815 1.00 7.45 DIC ATOM 1536 O ASN 193 27.355 43.977 78.926 1.00 9.83 DIC ATOM 1537 N GLY 194 25.798 43.099 77.556 1.00 7.11 DIC ATOM 1538 CA GLY 194 25.227 42.268 78.599 1.00 7.61 DIC ATOM 1539 C GLY 194 26.196 41.240 79.139 1.00 8.02 DIC ATOM 1540 O GLY 194 26.318 41.064 80.351 1.00 8.13 DIC ATOM 1541 N LEU 195 26.893 40.559 78.237 1.00 6.93 DIC ATOM 1542 CA LEU 195 27.851 39.539 78.632 1.00 8.13 DIC ATOM 1543 CB LEU 195 28.330 38.746 77.407 1.00 5.03 DIC ATOM 1544 CG LEU 195 27.361 37.849 76.641 1.00 6.16 DIC ATOM 1545 CD1 LEU 195 28.134 37.104 75.553 1.00 5.85 DIC ATOM 1546 CD2 LEU 195 26.693 36.861 77.591 1.00 6.84 DIC ATOM 1547 C LEU 195 29.086 40.077 79.349 1.00 7.32 DIC ATOM 1548 O LEU 195 29.555 39.478 80.314 1.00 6.97 DIC ATOM 1549 N PHE 196 29.609 41.205 78.882 1.00 8.32 DIC ATOM 1550 CA PHE 196 30.842 41.739 79.448 1.00 6.43 DIC ATOM 1551 CB PHE 196 31.788 42.122 78.302 1.00 7.48 DIC ATOM 1552 CG PHE 196 31.994 41.021 77.293 1.00 7.64 DIC ATOM 1553 CD1 PHE 196 32.079 39.694 77.702 1.00 7.32 DIC ATOM 1554 CD2 PHE 196 32.138 41.315 75.939 1.00 8.39 DIC ATOM 1555 CE1 PHE 196 32.309 38.669 76.783 1.00 9.53 DIC ATOM 1556 CE2 PHE 196 32.370 40.300 75.008 1.00 8.57 DIC ATOM 1557 CZ PHE 196 32.456 38.974 75.431 1.00 9.27 DIC ATOM 1558 C PHE 196 30.773 42.883 80.453 1.00 7.23 DIC ATOM 1559 O PHE 196 31.813 43.342 80.931 1.00 6.97 DIC ATOM 1560 N LYS 197 29.571 43.340 80.787 1.00 7.17 DIC ATOM 1561 CA LYS 197 29.430 44.428 81.745 1.00 7.37 DIC ATOM 1562 CB LYS 197 27.950 44.632 82.106 1.00 8.11 DIC ATOM 1563 CG LYS 197 27.239 43.431 82.719 1.00 9.34 DIC ATOM 1564 CD LYS 197 25.752 43.730 82.867 1.00 7.17 DIC ATOM 1565 CE LYS 197 24.991 42.602 83.562 1.00 9.65 DIC ATOM 1566 NZ LYS 197 25.011 41.324 82.791 1.00 9.78 DIC ATOM 1567 C LYS 197 30.260 44.164 83.001 1.00 8.15 DIC ATOM 1568 O LYS 197 30.289 43.049 83.517 1.00 6.36 DIC ATOM 1569 N GLY 198 30.951 45.194 83.478 1.00 8.63 DIC ATOM 1570 CA GLY 198 31.781 45.043 84.660 1.00 9.48 DIC ATOM 1571 C GLY 198 33.170 44.550 84.307 1.00 11.16 DIC ATOM 1572 O GLY 198 34.065 44.534 85.151 1.00 11.56 DIC ATOM 1573 N GLY 199 33.353 44.147 83.052 1.00 9.98 DIC ATOM 1574 CA GLY 199 34.649 43.656 82.617 1.00 10.95 DIC ATOM 1575 C GLY 199 35.067 44.312 81.315 1.00 11.00 DIC ATOM 1576 O GLY 199 35.598 43.659 80.420 1.00 10.44 DIC ATOM 1577 N VAL 200 34.823 45.614 81.217 1.00 9.87 DIC ATOM 1578 CA VAL 200 35.159 46.377 80.022 1.00 10.31 DIC ATOM 1579 CB VAL 200 33.890 47.027 79.405 1.00 9.97 DIC ATOM 1580 CG1 VAL 200 34.265 47.857 78.186 1.00 13.00 DIC ATOM 1581 CG2 VAL 200 32.884 45.955 79.018 1.00 9.98 DIC ATOM 1582 C VAL 200 36.157 47.492 80.315 1.00 9.00 DIC ATOM 1583 O VAL 200 36.037 48.197 81.316 1.00 9.62 DIC ATOM 1584 N CYS 201 37.149 47.633 79.443 1.00 10.08 DIC ATOM 1585 CA CYS 201 38.137 48.696 79.561 1.00 11.93 DIC ATOM 1586 CB CYS 201 39.508 48.204 79.102 1.00 16.16 DIC ATOM 1587 SG CYS 201 40.754 49.497 78.999 1.00 22.80 DIC ATOM 1588 C CYS 201 37.624 49.778 78.615 1.00 12.32 DIC ATOM 1589 O CYS 201 37.383 49.504 77.438 1.00 11.10 DIC ATOM 1590 N TYR 202 37.434 50.998 79.110 1.00 11.44 DIC ATOM 1591 CA TYR 202 36.914 52.051 78.245 1.00 11.56 DIC ATOM 1592 CB TYR 202 36.008 53.001 79.034 1.00 13.47 DIC ATOM 1593 CG TYR 202 34.888 52.317 79.784 1.00 12.77 DIC ATOM 1594 CD1 TYR 202 34.977 52.112 81.159 1.00 14.55 DIC ATOM 1595 CE1 TYR 202 33.950 51.501 81.865 1.00 15.50 DIC ATOM 1596 CD2 TYR 202 33.734 51.884 79.124 1.00 13.35 DIC ATOM 1597 CE2 TYR 202 32.695 51.263 79.824 1.00 13.55 DIC ATOM 1598 CZ TYR 202 32.815 51.080 81.197 1.00 14.96 DIC ATOM 1599 OH TYR 202 31.801 50.494 81.912 1.00 15.14 DIC ATOM 1600 C TYR 202 37.998 52.860 77.543 1.00 12.95 DIC ATOM 1601 O TYR 202 38.970 53.291 78.160 1.00 12.67 DIC ATOM 1602 N ALA 203 37.818 53.060 76.243 1.00 12.15 DIC ATOM 1603 CA ALA 203 38.762 53.829 75.443 1.00 12.67 DIC ATOM 1604 CB ALA 203 39.001 53.134 74.107 1.00 11.34 DIC ATOM 1605 C ALA 203 38.181 55.220 75.212 1.00 11.62 DIC ATOM 1606 O ALA 203 36.968 55.412 75.300 1.00 10.59 DIC ATOM 1607 N ASN 204 39.041 56.188 74.916 1.00 10.55 DIC ATOM 1608 CA ASN 204 38.575 57.550 74.669 1.00 9.36 DIC ATOM 1609 CB ASN 204 39.758 58.498 74.487 1.00 7.28 DIC ATOM 1610 CG ASN 204 39.333 59.943 74.432 1.00 9.32 DIC ATOM 1611 OD1 ASN 204 39.037 60.559 75.463 1.00 9.40 DIC ATOM 1612 ND2 ASN 204 39.281 60.494 73.226 1.00 5.22 DIC ATOM 1613 C ASN 204 37.711 57.566 73.411 1.00 8.45 DIC ATOM 1614 O ASN 204 37.921 56.771 72.493 1.00 8.52 DIC ATOM 1615 N SER 205 36.743 58.474 73.370 1.00 6.68 DIC ATOM 1616 CA SER 205 35.845 58.573 72.227 1.00 8.43 DIC ATOM 1617 CB SER 205 34.708 59.552 72.539 1.00 6.55 DIC ATOM 1618 OG SER 205 33.769 58.945 73.415 1.00 5.21 DIC ATOM 1619 C SER 205 36.520 58.947 70.908 1.00 8.25 DIC ATOM 1620 O SER 205 35.890 58.884 69.846 1.00 7.41 DIC ATOM 1621 N ARG 206 37.796 59.324 70.959 1.00 6.24 DIC ATOM 1622 CA ARG 206 38.503 59.664 69.727 1.00 5.53 DIC ATOM 1623 CB ARG 206 39.901 60.235 70.031 1.00 5.02 DIC ATOM 1624 CG ARG 206 40.916 59.262 70.645 1.00 3.89 DIC ATOM 1625 CD ARG 206 42.220 60.002 71.003 1.00 6.14 DIC ATOM 1626 NE ARG 206 42.757 60.730 69.852 1.00 5.51 DIC ATOM 1627 CZ ARG 206 43.820 60.352 69.145 1.00 6.07 DIC ATOM 1628 NH1 ARG 206 44.486 59.252 69.471 1.00 5.54 DIC ATOM 1629 NH2 ARG 206 44.196 61.056 68.086 1.00 3.75 DIC ATOM 1630 C ARG 206 38.625 58.421 68.844 1.00 4.90 DIC ATOM 1631 O ARG 206 38.815 58.525 67.632 1.00 5.35 DIC ATOM 1632 N PHE 207 38.501 57.246 69.455 1.00 4.24 DIC ATOM 1633 CA PHE 207 38.612 55.988 68.722 1.00 4.90 DIC ATOM 1634 CB PHE 207 39.326 54.945 69.588 1.00 4.86 DIC ATOM 1635 CG PHE 207 40.764 55.288 69.875 1.00 5.99 DIC ATOM 1636 CD1 PHE 207 41.176 55.620 71.162 1.00 5.64 DIC ATOM 1637 CD2 PHE 207 41.700 55.322 68.842 1.00 4.91 DIC ATOM 1638 CE1 PHE 207 42.497 55.983 71.417 1.00 7.00 DIC ATOM 1639 CE2 PHE 207 43.024 55.684 69.085 1.00 7.26 DIC ATOM 1640 CZ PHE 207 43.424 56.016 70.375 1.00 6.13 DIC ATOM 1641 C PHE 207 37.276 55.439 68.224 1.00 5.37 DIC ATOM 1642 O PHE 207 37.208 54.338 67.682 1.00 6.61 DIC ATOM 1643 N ASN 208 36.215 56.214 68.414 1.00 5.44 DIC ATOM 1644 CA ASN 208 34.882 55.831 67.963 1.00 7.19 DIC ATOM 1645 CB ASN 208 34.279 54.752 68.863 1.00 4.53 DIC ATOM 1646 CG ASN 208 33.112 54.038 68.201 1.00 4.94 DIC ATOM 1647 OD1 ASN 208 32.464 54.587 67.304 1.00 3.79 DIC ATOM 1648 ND2 ASN 208 32.832 52.814 68.645 1.00 3.51 DIC ATOM 1649 C ASN 208 34.037 57.094 68.026 1.00 7.68 DIC ATOM 1650 O ASN 208 33.170 57.241 68.888 1.00 7.11 DIC ATOM 1651 N PHE 209 34.315 57.998 67.093 1.00 6.81 DIC ATOM 1652 CA PHE 209 33.647 59.288 67.004 1.00 8.34 DIC ATOM 1653 CB PHE 209 34.636 60.315 66.439 1.00 8.19 DIC ATOM 1654 CG PHE 209 34.226 61.740 66.648 1.00 7.78 DIC ATOM 1655 CD1 PHE 209 34.260 62.308 67.918 1.00 8.92 DIC ATOM 1656 CD2 PHE 209 33.830 62.525 65.569 1.00 9.53 DIC ATOM 1657 CE1 PHE 209 33.907 63.644 68.112 1.00 11.27 DIC ATOM 1658 CE2 PHE 209 33.476 63.858 65.751 1.00 8.49 DIC ATOM 1659 CZ PHE 209 33.515 64.419 67.025 1.00 9.96 DIC ATOM 1660 C PHE 209 32.431 59.166 66.094 1.00 8.23 DIC ATOM 1661 O PHE 209 32.569 59.073 64.877 1.00 8.27 DIC ATOM 1662 N MSE 210 31.244 59.179 66.692 1.00 7.38 DIC ATOM 1663 CA MSE 210 29.999 59.037 65.941 1.00 9.26 DIC ATOM 1664 CB MSE 210 29.159 57.918 66.581 1.00 9.05 DIC ATOM 1665 CG MSE 210 29.866 56.564 66.584 1.00 10.93 DIC ATOM 1666 SE MSE 210 29.082 55.239 67.779 1.00 18.26 DIC ATOM 1667 CE MSE 210 30.053 55.690 69.381 1.00 8.17 DIC ATOM 1668 C MSE 210 29.195 60.338 65.870 1.00 8.65 DIC ATOM 1669 O MSE 210 29.562 61.340 66.486 1.00 6.86 DIC ATOM 1670 N PRO 211 28.086 60.343 65.105 1.00 9.68 DIC ATOM 1671 CD PRO 211 27.573 59.289 64.211 1.00 9.09 DIC ATOM 1672 CA PRO 211 27.266 61.554 64.990 1.00 9.29 DIC ATOM 1673 CB PRO 211 26.037 61.058 64.240 1.00 9.60 DIC ATOM 1674 CG PRO 211 26.637 60.064 63.296 1.00 10.03 DIC ATOM 1675 C PRO 211 26.918 62.189 66.335 1.00 10.27 DIC ATOM 1676 O PRO 211 26.973 63.413 66.482 1.00 10.62 DIC ATOM 1677 N THR 212 26.572 61.367 67.322 1.00 7.87 DIC ATOM 1678 CA THR 212 26.222 61.906 68.629 1.00 8.03 DIC ATOM 1679 CB THR 212 25.663 60.807 69.561 1.00 8.27 DIC ATOM 1680 OG1 THR 212 24.528 60.191 68.939 1.00 9.40 DIC ATOM 1681 CG2 THR 212 25.216 61.410 70.886 1.00 9.47 DIC ATOM 1682 C THR 212 27.422 62.594 69.285 1.00 8.51 DIC ATOM 1683 O THR 212 27.266 63.607 69.975 1.00 8.07 DIC ATOM 1684 N ASN 213 28.616 62.046 69.074 1.00 6.60 DIC ATOM 1685 CA ASN 213 29.827 62.641 69.628 1.00 7.57 DIC ATOM 1686 CB ASN 213 31.047 61.768 69.315 1.00 7.05 DIC ATOM 1687 CG ASN 213 30.968 60.395 69.967 1.00 5.69 DIC ATOM 1688 OD1 ASN 213 31.421 60.198 71.098 1.00 5.17 DIC ATOM 1689 ND2 ASN 213 30.379 59.443 69.259 1.00 2.99 DIC ATOM 1690 C ASN 213 30.007 64.017 68.990 1.00 9.85 DIC ATOM 1691 O ASN 213 30.326 64.991 69.666 1.00 11.63 DIC ATOM 1692 N TYR 214 29.801 64.082 67.679 1.00 10.25 DIC ATOM 1693 CA TYR 214 29.926 65.333 66.945 1.00 12.74 DIC ATOM 1694 CB TYR 214 29.671 65.103 65.451 1.00 15.29 DIC ATOM 1695 CG TYR 214 29.730 66.365 64.619 1.00 17.71 DIC ATOM 1696 CD1 TYR 214 30.950 66.894 64.203 1.00 19.79 DIC ATOM 1697 CE1 TYR 214 31.011 68.072 63.461 1.00 21.10 DIC ATOM 1698 CD2 TYR 214 28.564 67.049 64.271 1.00 19.74 DIC ATOM 1699 CE2 TYR 214 28.612 68.230 63.530 1.00 22.09 DIC ATOM 1700 CZ TYR 214 29.838 68.735 63.128 1.00 22.87 DIC ATOM 1701 OH TYR 214 29.892 69.901 62.393 1.00 24.30 DIC ATOM 1702 C TYR 214 28.922 66.347 67.481 1.00 13.83 DIC ATOM 1703 O TYR 214 29.276 67.490 67.761 1.00 12.55 DIC ATOM 1704 N ALA 215 27.669 65.923 67.625 1.00 15.46 DIC ATOM 1705 CA ALA 215 26.615 66.803 68.124 1.00 17.53 DIC ATOM 1706 CB ALA 215 25.271 66.081 68.099 1.00 15.12 DIC ATOM 1707 C ALA 215 26.919 67.288 69.539 1.00 19.46 DIC ATOM 1708 O ALA 215 26.509 68.381 69.931 1.00 19.21 DIC ATOM 1709 N ALA 216 27.639 66.471 70.300 1.00 21.21 DIC ATOM 1710 CA ALA 216 27.991 66.821 71.669 1.00 24.59 DIC ATOM 1711 CB ALA 216 28.459 65.580 72.421 1.00 23.56 DIC ATOM 1712 C ALA 216 29.069 67.905 71.713 1.00 27.77 DIC ATOM 1713 O ALA 216 29.317 68.497 72.762 1.00 27.20 DIC ATOM 1714 N MSE 217 29.703 68.166 70.573 1.00 31.06 DIC ATOM 1715 CA MSE 217 30.743 69.189 70.498 1.00 34.21 DIC ATOM 1716 CB MSE 217 31.385 69.208 69.107 1.00 35.99 DIC ATOM 1717 CG MSE 217 32.193 67.966 68.760 1.00 39.28 DIC ATOM 1718 SE MSE 217 33.550 67.557 70.080 1.00 45.10 DIC ATOM 1719 CE MSE 217 34.867 68.888 69.607 1.00 42.38 DIC ATOM 1720 C MSE 217 30.175 70.570 70.809 1.00 35.31 DIC ATOM 1721 O MSE 217 29.016 70.860 70.503 1.00 36.62 DIC ATOM 1722 N ALA 222 25.134 68.364 77.425 1.00 31.46 DIC ATOM 1723 CA ALA 222 24.583 68.352 78.775 1.00 31.66 DIC ATOM 1724 CB ALA 222 23.312 67.513 78.813 1.00 32.95 DIC ATOM 1725 C ALA 222 25.604 67.803 79.765 1.00 31.68 DIC ATOM 1726 O ALA 222 26.479 68.538 80.229 1.00 32.14 DIC ATOM 1727 N ALA 223 25.483 66.511 80.071 1.00 31.10 DIC ATOM 1728 CA ALA 223 26.370 65.807 81.003 1.00 30.32 DIC ATOM 1729 CB ALA 223 26.806 66.741 82.137 1.00 30.79 DIC ATOM 1730 C ALA 223 25.626 64.605 81.581 1.00 28.04 DIC ATOM 1731 O ALA 223 24.856 64.749 82.528 1.00 29.66 DIC ATOM 1732 N ALA 224 25.856 63.422 81.018 1.00 27.00 DIC ATOM 1733 CA ALA 224 25.171 62.219 81.490 1.00 25.23 DIC ATOM 1734 CB ALA 224 25.440 61.057 80.543 1.00 25.60 DIC ATOM 1735 C ALA 224 25.530 61.817 82.918 1.00 24.60 DIC ATOM 1736 O ALA 224 24.642 61.593 83.742 1.00 24.76 DIC ATOM 1737 N HIS 225 26.825 61.716 83.206 1.00 23.10 DIC ATOM 1738 CA HIS 225 27.297 61.330 84.534 1.00 21.99 DIC ATOM 1739 CB HIS 225 27.907 59.926 84.490 1.00 22.53 DIC ATOM 1740 CG HIS 225 26.949 58.857 84.064 1.00 22.70 DIC ATOM 1741 CD2 HIS 225 26.829 58.183 82.896 1.00 21.83 DIC ATOM 1742 ND1 HIS 225 25.966 58.364 84.894 1.00 21.91 DIC ATOM 1743 CE1 HIS 225 25.282 57.430 84.256 1.00 22.15 DIC ATOM 1744 NE2 HIS 225 25.786 57.301 83.041 1.00 21.79 DIC ATOM 1745 C HIS 225 28.357 62.307 85.039 1.00 21.96 DIC ATOM 1746 O HIS 225 29.052 62.940 84.243 1.00 21.13 DIC ATOM 1747 N THR 226 28.480 62.422 86.360 1.00 21.29 DIC ATOM 1748 CA THR 226 29.474 63.313 86.956 1.00 20.93 DIC ATOM 1749 CB THR 226 29.032 63.827 88.347 1.00 20.27 DIC ATOM 1750 OG1 THR 226 28.812 62.715 89.225 1.00 23.22 DIC ATOM 1751 CG2 THR 226 27.756 64.637 88.233 1.00 21.25 DIC ATOM 1752 C THR 226 30.790 62.562 87.108 1.00 19.54 DIC ATOM 1753 O THR 226 31.854 63.168 87.205 1.00 19.24 DIC ATOM 1754 N ASP 227 30.702 61.236 87.133 1.00 18.16 DIC ATOM 1755 CA ASP 227 31.875 60.379 87.256 1.00 17.84 DIC ATOM 1756 CB ASP 227 31.512 58.958 86.827 1.00 19.84 DIC ATOM 1757 CG ASP 227 32.706 58.030 86.808 1.00 20.03 DIC ATOM 1758 OD1 ASP 227 32.607 56.955 86.185 1.00 21.19 DIC ATOM 1759 OD2 ASP 227 33.740 58.369 87.420 1.00 22.49 DIC ATOM 1760 C ASP 227 33.028 60.889 86.386 1.00 18.14 DIC ATOM 1761 O ASP 227 32.904 60.971 85.165 1.00 16.47 DIC ATOM 1762 N PRO 228 34.167 61.233 87.006 1.00 17.73 DIC ATOM 1763 CD PRO 228 34.480 61.151 88.443 1.00 18.17 DIC ATOM 1764 CA PRO 228 35.321 61.731 86.250 1.00 17.33 DIC ATOM 1765 CB PRO 228 36.363 61.995 87.339 1.00 18.94 DIC ATOM 1766 CG PRO 228 35.980 61.034 88.425 1.00 20.23 DIC ATOM 1767 C PRO 228 35.827 60.772 85.172 1.00 16.87 DIC ATOM 1768 O PRO 228 36.297 61.209 84.122 1.00 15.06 DIC ATOM 1769 N LEU 229 35.737 59.470 85.428 1.00 15.80 DIC ATOM 1770 CA LEU 229 36.188 58.496 84.446 1.00 15.66 DIC ATOM 1771 CB LEU 229 36.155 57.079 85.033 1.00 16.65 DIC ATOM 1772 CG LEU 229 36.728 55.969 84.147 1.00 17.28 DIC ATOM 1773 CD1 LEU 229 37.236 54.824 85.008 1.00 18.64 DIC ATOM 1774 CD2 LEU 229 35.661 55.487 83.172 1.00 15.76 DIC ATOM 1775 C LEU 229 35.281 58.596 83.224 1.00 14.21 DIC ATOM 1776 O LEU 229 35.759 58.658 82.092 1.00 15.12 DIC ATOM 1777 N TYR 230 33.972 58.628 83.457 1.00 14.01 DIC ATOM 1778 CA TYR 230 33.017 58.739 82.363 1.00 11.87 DIC ATOM 1779 CB TYR 230 31.585 58.846 82.895 1.00 14.20 DIC ATOM 1780 CG TYR 230 30.544 58.919 81.794 1.00 11.26 DIC ATOM 1781 CD1 TYR 230 30.146 57.774 81.105 1.00 13.91 DIC ATOM 1782 CE1 TYR 230 29.222 57.840 80.061 1.00 10.82 DIC ATOM 1783 CD2 TYR 230 29.991 60.139 81.414 1.00 12.75 DIC ATOM 1784 CE2 TYR 230 29.066 60.218 80.371 1.00 12.59 DIC ATOM 1785 CZ TYR 230 28.688 59.062 79.700 1.00 12.84 DIC ATOM 1786 OH TYR 230 27.779 59.132 78.665 1.00 11.30 DIC ATOM 1787 C TYR 230 33.332 59.983 81.538 1.00 11.96 DIC ATOM 1788 O TYR 230 33.441 59.913 80.317 1.00 9.30 DIC ATOM 1789 N ARG 231 33.472 61.119 82.218 1.00 11.98 DIC ATOM 1790 CA ARG 231 33.770 62.390 81.558 1.00 13.86 DIC ATOM 1791 CB ARG 231 33.823 63.515 82.598 1.00 16.38 DIC ATOM 1792 CG ARG 231 32.472 63.840 83.225 1.00 19.41 DIC ATOM 1793 CD ARG 231 32.635 64.503 84.588 1.00 24.54 DIC ATOM 1794 NE ARG 231 33.603 65.598 84.574 1.00 30.72 DIC ATOM 1795 CZ ARG 231 33.449 66.731 83.895 1.00 31.79 DIC ATOM 1796 NH1 ARG 231 34.390 67.667 83.945 1.00 33.17 DIC ATOM 1797 NH2 ARG 231 32.357 66.934 83.172 1.00 34.16 DIC ATOM 1798 C ARG 231 35.082 62.340 80.779 1.00 13.10 DIC ATOM 1799 O ARG 231 35.179 62.861 79.666 1.00 12.39 DIC ATOM 1800 N ASP 232 36.097 61.724 81.372 1.00 12.75 DIC ATOM 1801 CA ASP 232 37.393 61.609 80.716 1.00 12.99 DIC ATOM 1802 CB ASP 232 38.396 60.936 81.656 1.00 14.85 DIC ATOM 1803 CG ASP 232 39.709 60.610 80.973 1.00 16.86 DIC ATOM 1804 OD1 ASP 232 39.794 59.558 80.306 1.00 18.36 DIC ATOM 1805 OD2 ASP 232 40.656 61.412 81.094 1.00 16.54 DIC ATOM 1806 C ASP 232 37.302 60.819 79.406 1.00 12.82 DIC ATOM 1807 O ASP 232 37.864 61.224 78.387 1.00 10.29 DIC ATOM 1808 N ARG 233 36.584 59.699 79.435 1.00 10.29 DIC ATOM 1809 CA ARG 233 36.452 58.853 78.256 1.00 10.00 DIC ATOM 1810 CB ARG 233 35.932 57.470 78.661 1.00 9.23 DIC ATOM 1811 CG ARG 233 36.782 56.750 79.704 1.00 9.41 DIC ATOM 1812 CD ARG 233 38.153 56.364 79.163 1.00 8.38 DIC ATOM 1813 NE ARG 233 38.825 55.417 80.047 1.00 11.90 DIC ATOM 1814 CZ ARG 233 39.366 55.731 81.221 1.00 15.57 DIC ATOM 1815 NH1 ARG 233 39.332 56.983 81.666 1.00 14.61 DIC ATOM 1816 NH2 ARG 233 39.920 54.782 81.966 1.00 13.98 DIC ATOM 1817 C ARG 233 35.549 59.431 77.165 1.00 10.24 DIC ATOM 1818 O ARG 233 35.814 59.244 75.975 1.00 9.03 DIC ATOM 1819 N THR 234 34.490 60.132 77.564 1.00 8.98 DIC ATOM 1820 CA THR 234 33.559 60.693 76.592 1.00 10.49 DIC ATOM 1821 CB THR 234 32.141 60.811 77.183 1.00 10.70 DIC ATOM 1822 OG1 THR 234 32.181 61.585 78.387 1.00 9.78 DIC ATOM 1823 CG2 THR 234 31.587 59.416 77.488 1.00 8.75 DIC ATOM 1824 C THR 234 33.993 62.035 76.016 1.00 11.41 DIC ATOM 1825 O THR 234 33.481 62.459 74.982 1.00 11.24 DIC ATOM 1826 N ASN 235 34.924 62.710 76.681 1.00 9.83 DIC ATOM 1827 CA ASN 235 35.418 63.968 76.148 1.00 12.54 DIC ATOM 1828 CB ASN 235 36.045 64.845 77.232 1.00 15.96 DIC ATOM 1829 CG ASN 235 36.643 66.120 76.663 1.00 20.34 DIC ATOM 1830 OD1 ASN 235 35.940 66.934 76.063 1.00 25.44 DIC ATOM 1831 ND2 ASN 235 37.948 66.295 76.838 1.00 22.52 DIC ATOM 1832 C ASN 235 36.488 63.561 75.151 1.00 11.14 DIC ATOM 1833 O ASN 235 37.586 63.169 75.536 1.00 11.10 DIC ATOM 1834 N THR 236 36.154 63.638 73.870 1.00 11.67 DIC ATOM 1835 CA THR 236 37.081 63.260 72.813 1.00 11.17 DIC ATOM 1836 CB THR 236 36.413 63.396 71.433 1.00 11.34 DIC ATOM 1837 OG1 THR 236 35.373 62.417 71.318 1.00 10.79 DIC ATOM 1838 CG2 THR 236 37.431 63.197 70.315 1.00 9.33 DIC ATOM 1839 C THR 236 38.355 64.090 72.827 1.00 11.07 DIC ATOM 1840 O THR 236 38.307 65.320 72.919 1.00 11.47 DIC ATOM 1841 N VAL 237 39.494 63.409 72.754 1.00 10.07 DIC ATOM 1842 CA VAL 237 40.785 64.086 72.729 1.00 12.15 DIC ATOM 1843 CB VAL 237 41.865 63.310 73.523 1.00 12.90 DIC ATOM 1844 CG1 VAL 237 43.208 64.035 73.423 1.00 13.23 DIC ATOM 1845 CG2 VAL 237 41.448 63.183 74.980 1.00 13.18 DIC ATOM 1846 C VAL 237 41.210 64.177 71.268 1.00 12.16 DIC ATOM 1847 O VAL 237 41.583 63.175 70.654 1.00 12.69 DIC ATOM 1848 N MSE 238 41.133 65.381 70.714 1.00 12.20 DIC ATOM 1849 CA MSE 238 41.495 65.611 69.320 1.00 12.91 DIC ATOM 1850 CB MSE 238 41.283 67.081 68.960 1.00 15.07 DIC ATOM 1851 CG MSE 238 39.831 67.539 69.018 1.00 19.98 DIC ATOM 1852 SE MSE 238 38.678 66.551 67.809 1.00 27.67 DIC ATOM 1853 CE MSE 238 37.206 66.207 69.005 1.00 27.27 DIC ATOM 1854 C MSE 238 42.942 65.221 69.044 1.00 12.33 DIC ATOM 1855 O MSE 238 43.784 65.268 69.938 1.00 12.98 DIC ATOM 1856 N PRO 239 43.248 64.827 67.795 1.00 11.27 DIC ATOM 1857 CD PRO 239 44.633 64.625 67.335 1.00 13.15 DIC ATOM 1858 CA PRO 239 42.314 64.730 66.667 1.00 11.13 DIC ATOM 1859 CB PRO 239 43.239 64.787 65.455 1.00 12.20 DIC ATOM 1860 CG PRO 239 44.434 64.051 65.942 1.00 12.26 DIC ATOM 1861 C PRO 239 41.507 63.437 66.693 1.00 11.12 DIC ATOM 1862 O PRO 239 41.875 62.481 67.381 1.00 11.27 DIC ATOM 1863 N VAL 240 40.406 63.411 65.947 1.00 10.78 DIC ATOM 1864 CA VAL 240 39.582 62.212 65.873 1.00 8.88 DIC ATOM 1865 CB VAL 240 38.332 62.435 64.987 1.00 10.97 DIC ATOM 1866 CG1 VAL 240 37.571 61.120 64.817 1.00 11.55 DIC ATOM 1867 CG2 VAL 240 37.428 63.490 65.617 1.00 10.39 DIC ATOM 1868 C VAL 240 40.464 61.143 65.239 1.00 8.25 DIC ATOM 1869 O VAL 240 41.174 61.419 64.273 1.00 8.08 DIC ATOM 1870 N ALA 241 40.448 59.939 65.802 1.00 5.68 DIC ATOM 1871 CA ALA 241 41.255 58.844 65.277 1.00 5.69 DIC ATOM 1872 CB ALA 241 41.887 58.055 66.424 1.00 5.65 DIC ATOM 1873 C ALA 241 40.389 57.929 64.424 1.00 6.50 DIC ATOM 1874 O ALA 241 40.853 57.370 63.431 1.00 4.72 DIC ATOM 1875 N VAL 242 39.124 57.786 64.809 1.00 6.23 DIC ATOM 1876 CA VAL 242 38.204 56.940 64.058 1.00 5.56 DIC ATOM 1877 CB VAL 242 37.989 55.571 64.759 1.00 5.40 DIC ATOM 1878 CG1 VAL 242 37.029 54.707 63.939 1.00 5.43 DIC ATOM 1879 CG2 VAL 242 39.325 54.859 64.941 1.00 6.26 DIC ATOM 1880 C VAL 242 36.838 57.583 63.879 1.00 6.91 DIC ATOM 1881 O VAL 242 36.149 57.868 64.860 1.00 6.73 DIC ATOM 1882 N SER 243 36.462 57.823 62.623 1.00 6.89 DIC ATOM 1883 CA SER 243 35.148 58.370 62.300 1.00 7.37 DIC ATOM 1884 CB SER 243 35.177 59.164 60.985 1.00 9.26 DIC ATOM 1885 OG SER 243 35.627 60.492 61.187 1.00 12.73 DIC ATOM 1886 C SER 243 34.248 57.153 62.120 1.00 7.64 DIC ATOM 1887 O SER 243 34.542 56.279 61.309 1.00 7.80 DIC ATOM 1888 N HIS 244 33.164 57.082 62.882 1.00 6.24 DIC ATOM 1889 CA HIS 244 32.247 55.952 62.779 1.00 7.04 DIC ATOM 1890 CB HIS 244 32.209 55.183 64.103 1.00 5.69 DIC ATOM 1891 CG HIS 244 31.327 53.973 64.075 1.00 5.79 DIC ATOM 1892 CD2 HIS 244 30.668 53.373 63.055 1.00 5.25 DIC ATOM 1893 ND1 HIS 244 31.040 53.235 65.204 1.00 5.99 DIC ATOM 1894 CE1 HIS 244 30.242 52.233 64.880 1.00 8.18 DIC ATOM 1895 NE2 HIS 244 30.001 52.294 63.583 1.00 4.85 DIC ATOM 1896 C HIS 244 30.853 56.464 62.424 1.00 6.27 DIC ATOM 1897 O HIS 244 30.195 57.118 63.230 1.00 7.86 DIC ATOM 1898 N TYR 245 30.410 56.148 61.213 1.00 6.95 DIC ATOM 1899 CA TYR 245 29.112 56.585 60.719 1.00 8.61 DIC ATOM 1900 CB TYR 245 29.187 56.715 59.198 1.00 9.86 DIC ATOM 1901 CG TYR 245 30.263 57.699 58.815 1.00 10.60 DIC ATOM 1902 CD1 TYR 245 30.062 59.070 58.974 1.00 12.04 DIC ATOM 1903 CE1 TYR 245 31.090 59.983 58.752 1.00 12.10 DIC ATOM 1904 CD2 TYR 245 31.524 57.262 58.411 1.00 12.41 DIC ATOM 1905 CE2 TYR 245 32.564 58.169 58.187 1.00 12.40 DIC ATOM 1906 CZ TYR 245 32.339 59.527 58.364 1.00 12.62 DIC ATOM 1907 OH TYR 245 33.364 60.428 58.185 1.00 13.88 DIC ATOM 1908 C TYR 245 27.988 55.658 61.147 1.00 9.69 DIC ATOM 1909 O TYR 245 27.229 55.142 60.319 1.00 9.49 DIC ATOM 1910 N CYS 246 27.895 55.471 62.461 1.00 9.14 DIC ATOM 1911 CA CYS 246 26.888 54.618 63.071 1.00 11.69 DIC ATOM 1912 CB CYS 246 27.054 54.634 64.595 1.00 11.19 DIC ATOM 1913 SG CYS 246 26.047 53.422 65.477 1.00 17.18 DIC ATOM 1914 C CYS 246 25.511 55.147 62.689 1.00 12.03 DIC ATOM 1915 O CYS 246 25.273 56.351 62.722 1.00 11.82 DIC ATOM 1916 N GLY 247 24.607 54.246 62.323 1.00 12.35 DIC ATOM 1917 CA GLY 247 23.275 54.674 61.940 1.00 12.18 DIC ATOM 1918 C GLY 247 23.036 54.572 60.443 1.00 13.09 DIC ATOM 1919 O GLY 247 23.949 54.244 59.685 1.00 12.04 DIC ATOM 1920 N PRO 248 21.811 54.874 59.985 1.00 14.33 DIC ATOM 1921 CD PRO 248 20.738 55.471 60.803 1.00 14.23 DIC ATOM 1922 CA PRO 248 21.412 54.819 58.575 1.00 15.43 DIC ATOM 1923 CB PRO 248 19.940 55.227 58.625 1.00 17.10 DIC ATOM 1924 CG PRO 248 19.912 56.199 59.769 1.00 16.43 DIC ATOM 1925 C PRO 248 22.214 55.678 57.594 1.00 14.95 DIC ATOM 1926 O PRO 248 22.395 55.294 56.441 1.00 15.51 DIC ATOM 1927 N ALA 249 22.692 56.832 58.044 1.00 15.80 DIC ATOM 1928 CA ALA 249 23.442 57.737 57.175 1.00 16.01 DIC ATOM 1929 CB ALA 249 23.403 59.152 57.748 1.00 17.18 DIC ATOM 1930 C ALA 249 24.889 57.294 56.964 1.00 16.42 DIC ATOM 1931 O ALA 249 25.748 57.533 57.811 1.00 16.26 DIC ATOM 1932 N LYS 250 25.152 56.658 55.825 1.00 14.75 DIC ATOM 1933 CA LYS 250 26.490 56.169 55.506 1.00 14.92 DIC ATOM 1934 CB LYS 250 26.407 54.766 54.901 1.00 11.81 DIC ATOM 1935 CG LYS 250 25.716 53.736 55.783 1.00 11.87 DIC ATOM 1936 CD LYS 250 26.383 53.603 57.153 1.00 10.01 DIC ATOM 1937 CE LYS 250 25.710 52.507 57.983 1.00 10.47 DIC ATOM 1938 NZ LYS 250 26.130 52.549 59.415 1.00 8.71 DIC ATOM 1939 C LYS 250 27.225 57.093 54.542 1.00 15.74 DIC ATOM 1940 O LYS 250 26.609 57.737 53.695 1.00 16.86 DIC ATOM 1941 N PRO 251 28.563 57.152 54.646 1.00 16.85 DIC ATOM 1942 CD PRO 251 29.427 56.337 55.520 1.00 16.47 DIC ATOM 1943 CA PRO 251 29.369 58.010 53.771 1.00 17.98 DIC ATOM 1944 CB PRO 251 30.782 57.836 54.326 1.00 16.79 DIC ATOM 1945 CG PRO 251 30.769 56.421 54.821 1.00 18.00 DIC ATOM 1946 C PRO 251 29.270 57.654 52.289 1.00 19.21 DIC ATOM 1947 O PRO 251 29.493 58.504 51.425 1.00 20.56 DIC ATOM 1948 N TRP 252 28.936 56.401 51.993 1.00 20.23 DIC ATOM 1949 CA TRP 252 28.807 55.966 50.604 1.00 20.95 DIC ATOM 1950 CB TRP 252 29.134 54.476 50.483 1.00 18.75 DIC ATOM 1951 CG TRP 252 28.377 53.604 51.431 1.00 15.29 DIC ATOM 1952 CD2 TRP 252 28.895 52.971 52.607 1.00 13.13 DIC ATOM 1953 CE2 TRP 252 27.839 52.236 53.185 1.00 11.47 DIC ATOM 1954 CE3 TRP 252 30.151 52.952 53.227 1.00 11.22 DIC ATOM 1955 CD1 TRP 252 27.065 53.243 51.347 1.00 14.01 DIC ATOM 1956 NE1 TRP 252 26.733 52.420 52.397 1.00 12.89 DIC ATOM 1957 CZ2 TRP 252 27.998 51.488 54.357 1.00 11.76 DIC ATOM 1958 CZ3 TRP 252 30.311 52.207 54.395 1.00 10.17 DIC ATOM 1959 CH2 TRP 252 29.239 51.486 54.945 1.00 9.82 DIC ATOM 1960 C TRP 252 27.415 56.249 50.046 1.00 23.17 DIC ATOM 1961 O TRP 252 27.069 55.808 48.948 1.00 24.13 DIC ATOM 1962 N HIS 253 26.620 56.990 50.809 1.00 24.69 DIC ATOM 1963 CA HIS 253 25.273 57.351 50.388 1.00 27.61 DIC ATOM 1964 CB HIS 253 24.364 57.523 51.605 1.00 26.78 DIC ATOM 1965 CG HIS 253 23.843 56.233 52.156 1.00 27.30 DIC ATOM 1966 CD2 HIS 253 23.890 54.972 51.666 1.00 26.61 DIC ATOM 1967 ND1 HIS 253 23.147 56.159 53.343 1.00 27.44 DIC ATOM 1968 CE1 HIS 253 22.786 54.907 53.561 1.00 27.37 DIC ATOM 1969 NE2 HIS 253 23.224 54.167 52.559 1.00 27.99 DIC ATOM 1970 C HIS 253 25.293 58.645 49.582 1.00 29.67 DIC ATOM 1971 O HIS 253 24.324 58.968 48.892 1.00 14.02 DIC ATOM 1972 N ALA 258 27.264 63.867 56.914 1.00 29.28 DIC ATOM 1973 CA ALA 258 27.941 63.637 58.185 1.00 27.86 DIC ATOM 1974 CB ALA 258 27.889 62.162 58.545 1.00 26.95 DIC ATOM 1975 C ALA 258 29.388 64.107 58.096 1.00 26.15 DIC ATOM 1976 O ALA 258 29.995 64.081 57.026 1.00 26.60 DIC ATOM 1977 N TRP 259 29.933 64.540 59.228 1.00 25.33 DIC ATOM 1978 CA TRP 259 31.305 65.026 59.282 1.00 24.17 DIC ATOM 1979 CB TRP 259 31.678 65.406 60.716 1.00 24.67 DIC ATOM 1980 CG TRP 259 33.088 65.907 60.841 1.00 24.17 DIC ATOM 1981 CD2 TRP 259 34.222 65.166 61.307 1.00 23.57 DIC ATOM 1982 CE2 TRP 259 35.347 66.012 61.199 1.00 24.08 DIC ATOM 1983 CE3 TRP 259 34.398 63.867 61.803 1.00 23.76 DIC ATOM 1984 CD1 TRP 259 33.556 67.137 60.482 1.00 24.26 DIC ATOM 1985 NE1 TRP 259 34.913 67.209 60.693 1.00 24.21 DIC ATOM 1986 CZ2 TRP 259 36.633 65.602 61.571 1.00 24.47 DIC ATOM 1987 CZ3 TRP 259 35.678 63.459 62.172 1.00 21.73 DIC ATOM 1988 CH2 TRP 259 36.776 64.324 62.054 1.00 23.77 DIC ATOM 1989 C TRP 259 32.319 64.006 58.770 1.00 24.50 DIC ATOM 1990 O TRP 259 32.183 62.804 59.006 1.00 24.08 DIC ATOM 1991 N GLY 260 33.333 64.503 58.065 1.00 22.84 DIC ATOM 1992 CA GLY 260 34.389 63.651 57.545 1.00 22.82 DIC ATOM 1993 C GLY 260 34.026 62.699 56.421 1.00 22.52 DIC ATOM 1994 O GLY 260 34.883 61.959 55.944 1.00 22.25 DIC ATOM 1995 N ALA 261 32.769 62.713 55.992 1.00 23.04 DIC ATOM 1996 CA ALA 261 32.324 61.830 54.923 1.00 22.66 DIC ATOM 1997 CB ALA 261 30.849 62.081 54.623 1.00 24.10 DIC ATOM 1998 C ALA 261 33.156 61.989 53.648 1.00 23.16 DIC ATOM 1999 O ALA 261 33.369 61.023 52.915 1.00 24.06 DIC ATOM 2000 N ALA 262 33.628 63.205 53.388 1.00 22.44 DIC ATOM 2001 CA ALA 262 34.423 63.489 52.194 1.00 21.08 DIC ATOM 2002 CB ALA 262 34.829 64.960 52.174 1.00 22.66 DIC ATOM 2003 C ALA 262 35.663 62.616 52.058 1.00 20.72 DIC ATOM 2004 O ALA 262 36.129 62.368 50.943 1.00 18.77 DIC ATOM 2005 N ARG 263 36.208 62.163 53.184 1.00 18.78 DIC ATOM 2006 CA ARG 263 37.397 61.318 53.153 1.00 18.76 DIC ATOM 2007 CB ARG 263 37.924 61.067 54.570 1.00 21.15 DIC ATOM 2008 CG ARG 263 39.094 60.079 54.635 1.00 25.36 DIC ATOM 2009 CD ARG 263 39.670 59.996 56.051 1.00 30.63 DIC ATOM 2010 NE ARG 263 40.709 58.973 56.199 1.00 32.82 DIC ATOM 2011 CZ ARG 263 41.814 58.901 55.460 1.00 34.60 DIC ATOM 2012 NH1 ARG 263 42.696 57.933 55.681 1.00 34.80 DIC ATOM 2013 NH2 ARG 263 42.037 59.785 54.495 1.00 34.28 DIC ATOM 2014 C ARG 263 37.089 59.991 52.478 1.00 17.13 DIC ATOM 2015 O ARG 263 37.963 59.384 51.862 1.00 16.27 DIC ATOM 2016 N PHE 264 35.844 59.540 52.599 1.00 15.52 DIC ATOM 2017 CA PHE 264 35.437 58.284 51.983 1.00 15.68 DIC ATOM 2018 CB PHE 264 33.970 57.978 52.293 1.00 15.52 DIC ATOM 2019 CG PHE 264 33.495 56.678 51.716 1.00 14.73 DIC ATOM 2020 CD1 PHE 264 33.570 55.504 52.459 1.00 15.37 DIC ATOM 2021 CD2 PHE 264 33.009 56.617 50.412 1.00 14.26 DIC ATOM 2022 CE1 PHE 264 33.170 54.289 51.915 1.00 14.89 DIC ATOM 2023 CE2 PHE 264 32.606 55.405 49.856 1.00 13.60 DIC ATOM 2024 CZ PHE 264 32.687 54.239 50.609 1.00 14.32 DIC ATOM 2025 C PHE 264 35.611 58.372 50.469 1.00 16.23 DIC ATOM 2026 O PHE 264 36.271 57.529 49.858 1.00 16.76 DIC ATOM 2027 N THR 265 35.014 59.398 49.870 1.00 17.19 DIC ATOM 2028 CA THR 265 35.092 59.587 48.426 1.00 19.52 DIC ATOM 2029 CB THR 265 34.227 60.789 47.970 1.00 21.53 DIC ATOM 2030 OG1 THR 265 34.141 60.802 46.538 1.00 24.56 DIC ATOM 2031 CG2 THR 265 34.832 62.095 48.437 1.00 22.63 DIC ATOM 2032 C THR 265 36.539 59.788 47.971 1.00 19.59 DIC ATOM 2033 O THR 265 36.938 59.308 46.910 1.00 18.82 DIC ATOM 2034 N GLU 266 37.331 60.485 48.780 1.00 18.91 DIC ATOM 2035 CA GLU 266 38.729 60.710 48.435 1.00 19.77 DIC ATOM 2036 CB GLU 266 39.394 61.635 49.450 1.00 22.93 DIC ATOM 2037 CG GLU 266 40.890 61.785 49.227 1.00 29.46 DIC ATOM 2038 CD GLU 266 41.516 62.808 50.146 1.00 32.08 DIC ATOM 2039 OE1 GLU 266 41.433 62.632 51.380 1.00 34.07 DIC ATOM 2040 OE2 GLU 266 42.091 63.790 49.631 1.00 35.23 DIC ATOM 2041 C GLU 266 39.488 59.386 48.384 1.00 18.19 DIC ATOM 2042 O GLU 266 40.345 59.185 47.525 1.00 16.67 DIC ATOM 2043 N LEU 267 39.177 58.488 49.315 1.00 16.93 DIC ATOM 2044 CA LEU 267 39.823 57.181 49.362 1.00 15.79 DIC ATOM 2045 CB LEU 267 39.571 56.509 50.715 1.00 17.37 DIC ATOM 2046 CG LEU 267 40.497 56.943 51.851 1.00 16.52 DIC ATOM 2047 CD1 LEU 267 40.007 56.374 53.165 1.00 17.75 DIC ATOM 2048 CD2 LEU 267 41.911 56.466 51.549 1.00 16.20 DIC ATOM 2049 C LEU 267 39.320 56.279 48.243 1.00 15.71 DIC ATOM 2050 O LEU 267 40.096 55.550 47.623 1.00 14.15 DIC ATOM 2051 N ALA 268 38.018 56.330 47.984 1.00 16.10 DIC ATOM 2052 CA ALA 268 37.430 55.511 46.932 1.00 18.09 DIC ATOM 2053 CB ALA 268 35.919 55.683 46.915 1.00 18.61 DIC ATOM 2054 C ALA 268 38.019 55.901 45.581 1.00 19.91 DIC ATOM 2055 O ALA 268 38.128 55.072 44.680 1.00 20.47 DIC ATOM 2056 N GLY 269 38.404 57.165 45.447 1.00 20.77 DIC ATOM 2057 CA GLY 269 38.974 57.627 44.196 1.00 22.67 DIC ATOM 2058 C GLY 269 40.431 57.241 44.014 1.00 23.70 DIC ATOM 2059 O GLY 269 40.946 57.266 42.898 1.00 24.52 DIC ATOM 2060 N SER 270 41.096 56.879 45.107 1.00 24.12 DIC ATOM 2061 CA SER 270 42.505 56.498 45.054 1.00 24.97 DIC ATOM 2062 CB SER 270 43.210 56.903 46.350 1.00 25.49 DIC ATOM 2063 OG SER 270 42.733 56.143 47.448 1.00 27.01 DIC ATOM 2064 C SER 270 42.687 55.001 44.842 1.00 25.34 DIC ATOM 2065 O SER 270 43.813 54.511 44.769 1.00 25.69 DIC ATOM 2066 N LEU 271 41.578 54.276 44.742 1.00 25.34 DIC ATOM 2067 CA LEU 271 41.633 52.834 44.558 1.00 25.82 DIC ATOM 2068 CB LEU 271 40.218 52.247 44.564 1.00 24.31 DIC ATOM 2069 CG LEU 271 39.497 52.396 45.907 1.00 23.12 DIC ATOM 2070 CD1 LEU 271 38.112 51.772 45.833 1.00 23.63 DIC ATOM 2071 CD2 LEU 271 40.328 51.732 46.999 1.00 21.99 DIC ATOM 2072 C LEU 271 42.370 52.410 43.295 1.00 26.79 DIC ATOM 2073 O LEU 271 42.110 52.916 42.205 1.00 26.57 DIC ATOM 2074 N THR 272 43.297 51.474 43.469 1.00 27.68 DIC ATOM 2075 CA THR 272 44.099 50.940 42.378 1.00 28.62 DIC ATOM 2076 CB THR 272 45.090 49.884 42.902 1.00 28.86 DIC ATOM 2077 OG1 THR 272 45.988 50.496 43.835 1.00 31.54 DIC ATOM 2078 CG2 THR 272 45.882 49.278 41.757 1.00 29.83 DIC ATOM 2079 C THR 272 43.219 50.290 41.320 1.00 28.48 DIC ATOM 2080 O THR 272 43.315 50.615 40.136 1.00 27.52 DIC ATOM 2081 N THR 273 42.368 49.366 41.759 1.00 28.31 DIC ATOM 2082 CA THR 273 41.463 48.649 40.867 1.00 27.75 DIC ATOM 2083 CB THR 273 41.776 47.136 40.851 1.00 29.35 DIC ATOM 2084 OG1 THR 273 43.155 46.931 40.515 1.00 31.31 DIC ATOM 2085 CG2 THR 273 40.900 46.426 39.828 1.00 31.25 DIC ATOM 2086 C THR 273 40.018 48.824 41.324 1.00 25.84 DIC ATOM 2087 O THR 273 39.695 48.590 42.489 1.00 24.34 DIC ATOM 2088 N VAL 274 39.151 49.230 40.402 1.00 22.69 DIC ATOM 2089 CA VAL 274 37.745 49.425 40.725 1.00 20.88 DIC ATOM 2090 CB VAL 274 37.378 50.932 40.744 1.00 19.63 DIC ATOM 2091 CG1 VAL 274 37.700 51.569 39.405 1.00 21.82 DIC ATOM 2092 CG2 VAL 274 35.906 51.106 41.077 1.00 20.86 DIC ATOM 2093 C VAL 274 36.851 48.684 39.735 1.00 19.45 DIC ATOM 2094 O VAL 274 36.644 49.129 38.604 1.00 19.49 DIC ATOM 2095 N PRO 275 36.317 47.524 40.151 1.00 18.18 DIC ATOM 2096 CD PRO 275 36.580 46.851 41.433 1.00 16.49 DIC ATOM 2097 CA PRO 275 35.441 46.705 39.311 1.00 17.39 DIC ATOM 2098 CB PRO 275 35.079 45.540 40.230 1.00 17.76 DIC ATOM 2099 CG PRO 275 36.283 45.416 41.097 1.00 17.23 DIC ATOM 2100 C PRO 275 34.208 47.476 38.858 1.00 16.95 DIC ATOM 2101 O PRO 275 33.642 48.257 39.619 1.00 14.46 DIC ATOM 2102 N GLU 276 33.799 47.257 37.613 1.00 18.62 DIC ATOM 2103 CA GLU 276 32.620 47.924 37.070 1.00 19.68 DIC ATOM 2104 CB GLU 276 32.250 47.292 35.720 1.00 20.05 DIC ATOM 2105 CG GLU 276 30.884 47.680 35.146 1.00 23.31 DIC ATOM 2106 CD GLU 276 30.747 49.162 34.846 1.00 24.44 DIC ATOM 2107 OE1 GLU 276 31.776 49.825 34.606 1.00 25.94 DIC ATOM 2108 OE2 GLU 276 29.601 49.662 34.834 1.00 26.03 DIC ATOM 2109 C GLU 276 31.453 47.812 38.056 1.00 19.58 DIC ATOM 2110 O GLU 276 30.705 48.765 38.255 1.00 19.51 DIC ATOM 2111 N GLU 277 31.325 46.651 38.693 1.00 19.98 DIC ATOM 2112 CA GLU 277 30.246 46.413 39.647 1.00 21.58 DIC ATOM 2113 CB GLU 277 30.155 44.916 39.962 1.00 25.97 DIC ATOM 2114 CG GLU 277 28.727 44.372 40.027 1.00 31.33 DIC ATOM 2115 CD GLU 277 28.073 44.244 38.653 1.00 33.58 DIC ATOM 2116 OE1 GLU 277 27.923 45.267 37.948 1.00 34.50 DIC ATOM 2117 OE2 GLU 277 27.706 43.111 38.279 1.00 36.07 DIC ATOM 2118 C GLU 277 30.383 47.210 40.953 1.00 21.12 DIC ATOM 2119 O GLU 277 29.507 47.148 41.816 1.00 21.31 DIC ATOM 2120 N TRP 278 31.481 47.949 41.097 1.00 19.40 DIC ATOM 2121 CA TRP 278 31.719 48.772 42.286 1.00 18.57 DIC ATOM 2122 CB TRP 279 33.174 48.652 42.744 1.00 16.02 DIC ATOM 2123 CG TRP 278 33.510 47.418 43.518 1.00 13.84 DIC ATOM 2124 CD2 TRP 278 34.666 47.224 44.339 1.00 13.65 DIC ATOM 2125 CE2 TRP 278 34.617 45.899 44.823 1.00 12.87 DIC ATOM 2126 CE3 TRP 278 35.742 48.042 44.711 1.00 11.77 DIC ATOM 2127 CD1 TRP 278 32.822 46.240 43.539 1.00 13.38 DIC ATOM 2128 NE1 TRP 278 33.481 45.321 44.321 1.00 14.26 DIC ATOM 2129 CZ2 TRP 278 35.604 45.371 45.661 1.00 11.66 DIC ATOM 2130 CZ3 TRP 278 36.724 47.516 45.546 1.00 12.57 DIC ATOM 2131 CH2 TRP 278 36.646 46.192 46.010 1.00 11.95 DIC ATOM 2132 C TRP 278 31.443 50.240 41.977 1.00 19.09 DIC ATOM 2133 O TRP 278 31.266 51.051 42.885 1.00 17.92 DIC ATOM 2134 N ALA 279 31.422 50.572 40.690 1.00 21.02 DIC. ATOM 2135 CA ALA 279 31.200 51.943 40.235 1.00 23.01 DIC ATOM 2136 CB ALA 279 31.061 51.969 38.717 1.00 24.70 DIC ATOM 2137 C ALA 279 29.997 52.619 40.875 1.00 23.44 DIC ATOM 2138 O ALA 279 30.088 53.764 41.317 1.00 25.20 DIC ATOM 2139 N ALA 280 28.871 51.917 40.918 1.00 24.09 DIC ATOM 2140 CA ALA 280 27.656 52.470 41.504 1.00 24.89 DIC ATOM 2141 CB ALA 280 26.460 51.598 41.140 1.00 25.25 DIC ATOM 2142 C ALA 280 27.765 52.604 43.024 1.00 25.44 DIC ATOM 2143 O ALA 280 27.449 53.655 43.586 1.00 26.12 DIC ATOM 2144 N ALA 281 28.214 51.538 43.680 1.00 24.53 DIC ATOM 2145 CA ALA 281 28.363 51.529 45.132 1.00 24.14 DIC ATOM 2146 CB ALA 281 28.895 50.176 45.592 1.00 22.30 DIC ATOM 2147 C ALA 281 29.301 52.637 45.590 1.00 24.69 DIC ATOM 2148 O ALA 281 29.097 53.231 46.649 1.00 24.21 DIC ATOM 2149 N ALA 282 30.326 52.890 44.775 1.00 25.23 DIC ATOM 2150 CA ALA 282 31.354 53.907 45.008 1.00 28.24 DIC ATOM 2151 CB ALA 282 30.889 54.936 46.040 1.00 29.57 DIC ATOM 2152 C ALA 282 32.672 53.285 45.456 1.00 29.28 DIC ATOM 2153 OT1 ALA 282 32.749 52.040 45.554 1.00 30.11 DIC ATOM 2154 OT2 ALA 282 33.619 54.061 45.703 1.00 31.66 DIC ATOM 2155 N1 UPG 341 27.143 44.459 57.507 1.00 10.01 ATOM 2156 C2 UPG 341 27.525 43.800 56.322 1.00 9.52 ATOM 2157 N3 UPG 341 26.652 44.070 55.245 1.00 8.67 ATOM 2158 C4 UPG 341 25.480 44.911 55.273 1.00 8.79 ATOM 2159 C5 UPG 341 25.173 45.541 56.522 1.00 8.07 ATOM 2160 C6 UPG 341 25.965 45.316 57.564 1.00 8.80 ATOM 2161 O2 UPG 341 28.508 43.077 56.249 1.00 9.10 ATOM 2162 O4 UPG 341 24.821 45.047 54.262 1.00 10.92 ATOM 2163 C4* UPG 341 28.064 45.814 60.802 1.00 9.49 ATOM 2164 O4* UPG 341 27.241 44.769 60.117 1.00 9.77 ATOM 2165 C3* UPG 341 28.852 46.439 59.647 1.00 8.11 ATOM 2166 O3* UPG 341 29.963 47.181 60.117 1.00 10.37 ATOM 2167 C2* UPG 341 29.109 45.217 58.781 1.00 9.07 ATOM 2168 O2* UPG 341 30.227 44.448 59.212 1.00 9.05 ATOM 2169 C1* UPG 341 27.829 44.408 58.886 1.00 10.20 ATOM 2170 C5* UPG 341 26.745 46.233 61.382 1.00 8.16 ATOM 2171 O5* UPG 341 26.201 47.589 61.086 1.00 14.00 ATOM 2172 PA UPG 341 26.684 49.097 60.762 1.00 11.18 ATOM 2173 O1A UPG 341 28.145 49.287 60.708 1.00 12.79 ATOM 2174 O2A UPG 341 25.988 49.605 59.534 1.00 13.97 ATOM 2175 O3A UPG 341 25.956 49.273 62.186 1.00 12.14 ATOM 2176 PB UPG 341 25.671 50.458 63.209 1.00 14.34 ATOM 2177 O1B UPG 341 26.996 51.096 63.328 1.00 11.37 ATOM 2178 O2B UPG 341 24.689 51.364 62.606 1.00 15.46 ATOM 2179 O3B UPG 341 25.195 49.937 64.603 1.00 15.30 ATOM 2180 C1′ UPG 341 25.560 49.791 66.150 1.00 20.50 ATOM 2181 C2′ UPG 341 27.035 49.261 66.121 1.00 19.24 ATOM 2182 C3′ UPG 341 27.359 48.017 65.147 1.00 20.09 ATOM 2183 C4′ UPG 341 26.330 46.877 65.447 1.00 19.60 ATOM 2184 C5′ UPG 341 24.895 47.560 65.400 1.00 19.91 ATOM 2185 C6′ UPG 341 23.873 46.533 65.880 1.00 21.17 ATOM 2186 F2′ UPG 341 27.959 50.293 65.853 1.00 22.12 ATOM 2187 O3′ UPG 341 28.644 47.531 65.431 1.00 18.85 ATOM 2188 O4′ UPG 341 26.604 46.316 66.765 1.00 17.85 ATOM 2189 O5′ UPG 341 24.675 48.684 66.396 1.00 19.90 ATOM 2190 O6′ UPG 341 23.634 45.281 65.305 1.00 20.17 ATOM 2191 MN MN 400 28.972 50.701 62.315 1.00 5.95 MN ATOM 2192 O HOH 500 33.706 51.230 70.721 1.00 5.79 ATOM 2193 O HOH 501 34.343 56.571 75.304 1.00 6.75 ATOM 2194 O HOH 502 17.802 43.967 68.994 1.00 10.59 ATOM 2195 O HOH 503 30.228 40.611 62.764 1.00 5.01 ATOM 2196 O HOH 504 39.307 27.582 66.202 1.00 10.52 ATOM 2197 O HOH 505 28.063 58.310 70.871 1.00 11.73 ATOM 2198 O HOH 506 28.710 46.590 79.022 1.00 6.65 ATOM 2199 O HOH 507 52.557 49.070 68.969 1.00 12.93 ATOM 2200 O HOH 508 45.198 58.379 72.300 1.00 14.17 ATOM 2201 O HOH 509 34.051 65.873 73.044 1.00 11.35 ATOM 2202 O HOH 510 41.782 55.536 74.876 1.00 9.63 ATOM 2203 O HOH 511 34.074 33.978 70.193 1.00 11.60 ATOM 2204 O HOH 512 26.575 37.907 50.900 1.00 12.73 ATOM 2205 O HOH 513 20.508 53.715 78.759 1.00 13.23 ATOM 2206 O HOH 514 51.349 46.691 65.666 1.00 17.16 ATOM 2207 O HOH 515 46.546 58.564 67.349 1.00 8.65 ATOM 2208 O HOH 516 52.691 53.505 61.177 1.00 12.18 ATOM 2209 O HOH 517 32.821 62.545 72.466 1.00 11.60 ATOM 2210 O HOH 518 25.540 58.412 67.321 1.00 14.19 ATOM 2211 O HOH 519 43.067 31.129 75.720 1.00 15.28 ATOM 2212 O HOH 520 42.729 59.876 74.613 1.00 15.64 ATOM 2213 O HOH 521 22.179 51.497 64.101 1.00 18.51 ATOM 2214 O HOH 522 34.014 47.551 83.195 1.00 9.04 ATOM 2215 O HOH 523 31.143 47.689 82.928 1.00 12.50 ATOM 2216 O HOH 524 32.337 57.530 71.624 1.00 8.71 ATOM 2217 O HOH 525 32.452 44.011 37.817 1.00 14.80 ATOM 2218 O HOH 526 24.863 45.001 86.150 1.00 15.13 ATOM 2219 O HOH 527 30.407 45.125 46.996 1.00 21.84 ATOM 2220 O HOH 528 20.754 39.640 56.706 1.00 9.45 ATOM 2221 O HOH 529 38.854 52.122 81.581 1.00 10.97 ATOM 2222 O HOH 530 40.378 59.034 77.824 1.00 17.34 ATOM 2223 O HOH 531 45.109 40.792 78.558 1.00 18.88 ATOM 2224 O HOH 532 48.994 58.795 68.032 1.00 18.00 ATOM 2225 O HOH 533 40.483 67.706 72.634 1.00 23.92 ATOM 2226 O HOH 534 41.280 60.433 45.444 1.00 22.17 ATOM 2227 O HOH 535 26.497 64.111 54.278 1.00 24.53 ATOM 2228 O HOH 536 45.960 43.860 76.459 1.00 17.37 ATOM 2229 O HOH 537 14.734 48.868 65.365 1.00 18.59 ATOM 2230 O HOH 538 46.131 38.545 57.874 1.00 24.34 ATOM 2231 O HOH 539 28.264 60.048 87.951 1.00 24.52 ATOM 2232 O HOH 540 46.748 45.401 73.816 1.00 16.95 ATOM 2233 O HOH 541 37.416 49.298 83.116 1.00 21.65 ATOM 2234 O HOH 542 27.237 60.848 55.024 1.00 18.79 ATOM 2235 O HOH 543 19.040 32.149 71.513 1.00 19.39 ATOM 2236 O HOH 544 24.859 59.199 87.172 1.00 21.96 ATOM 2237 O HOH 545 31.727 30.205 70.890 1.00 15.96 ATOM 2238 O HOH 546 50.448 55.331 62.596 1.00 19.00 ATOM 2239 O HOH 547 44.684 61.061 73.050 1.00 18.55 ATOM 2240 O HOH 548 23.917 28.286 65.355 1.00 22.75 ATOM 2241 O HOH 549 48.030 45.080 55.012 1.00 18.04 ATOM 2242 O HOH 550 31.863 50.861 84.807 1.00 12.35 ATOM 2243 O HOH 551 47.230 50.648 79.238 1.00 20.70 ATOM 2244 O HOH 552 45.574 59.143 57.227 1.00 26.33 ATOM 2245 O HOH 553 30.141 30.242 60.911 1.00 18.49 ATOM 2246 O HOH 554 39.361 63.494 77.807 1.00 19.60 ATOM 2247 O HOH 555 47.878 40.139 68.058 1.00 19.90 ATOM 2248 O HOH 556 33.763 51.759 54.205 1.00 21.40 ATOM 2249 O HOH 557 26.346 51.553 89.495 1.00 25.04 ATOM 2250 O HOH 558 43.622 40.021 44.147 1.00 18.14 ATOM 2251 O HOH 559 22.590 60.674 51.245 1.00 20.28 ATOM 2252 O HOH 560 46.899 45.705 42.406 1.00 23.24 ATOM 2253 O HOH 561 22.785 41.493 81.141 1.00 16.19 ATOM 2254 O HOH 562 24.738 38.970 55.796 1.00 22.33 ATOM 2255 O HOH 563 44.428 51.002 46.157 1.00 14.80 ATOM 2256 O HOH 564 24.412 40.573 48.290 1.00 23.85 ATOM 2257 O HOH 565 28.192 56.913 87.234 1.00 17.82 ATOM 2258 O HOH 566 49.326 45.339 71.775 1.00 22.08 ATOM 2259 O HOH 567 13.438 46.500 69.972 1.00 21.87 ATOM 2260 O HOH 568 36.472 30.850 71.825 1.00 24.81 ATOM 2261 O HOH 569 48.009 36.876 62.329 1.00 23.86 ATOM 2262 O HOH 570 24.860 62.779 55.872 1.00 26.97 ATOM 2263 O HOH 571 33.245 67.145 56.945 1.00 20.42 ATOM 2264 O HOH 572 42.157 34.486 52.245 1.00 16.87 ATOM 2265 O HOH 573 50.717 47.209 75.899 1.00 22.49 ATOM 2266 O HOH 574 29.865 33.602 47.244 1.00 32.56 ATOM 2267 O HOH 575 22.722 37.430 81.986 1.00 23.93 ATOM 2268 O HOH 576 50.100 42.319 65.178 1.00 22.32 ATOM 2269 O HOH 577 57.571 51.761 56.046 1.00 21.27 ATOM 2270 O HOH 578 47.296 51.529 51.324 1.00 20.20 ATOM 2271 O HOH 579 29.733 32.008 53.762 1.00 26.39 ATOM 2272 O HOH 580 26.968 35.843 81.316 1.00 22.87 ATOM 2273 O HOH 581 14.080 40.066 63.324 1.00 21.92 ATOM 2274 O HOH 582 28.224 49.947 38.771 1.00 25.67 ATOM 2275 O HOH 583 31.203 53.364 87.667 1.00 15.87 ATOM 2276 O HOH 584 42.912 37.536 80.236 1.00 23.43 ATOM 2277 O HOH 585 22.186 39.308 53.880 1.00 20.38 ATOM 2278 O HOH 586 48.511 56.150 75.023 1.00 32.95 ATOM 2279 O HOH 587 24.730 34.535 78.912 1.00 18.02 ATOM 2280 O HOH 588 32.604 39.346 83.395 1.00 22.21 ATOM 2281 O HOH 589 41.240 63.564 62.618 1.00 10.36 ATOM 2282 O HOH 590 26.537 56.699 69.106 1.00 8.22 ATOM 2283 O HOH 591 52.797 47.471 74.334 1.00 9.21 ATOM 2284 O HOH 592 41.777 32.558 61.182 1.00 10.73 ATOM 2285 O HOH 593 33.437 44.877 60.209 1.00 7.34 ATOM 2286 O HOH 594 33.888 31.650 71.550 1.00 14.92 ATOM 2287 O HOH 595 25.462 40.367 50.723 1.00 11.84 ATOM 2288 O HOH 596 43.591 57.443 74.474 1.00 17.30 ATOM 2289 O HOH 597 33.115 35.658 41.851 1.00 14.12 ATOM 2290 O HOH 598 44.433 41.685 76.122 1.00 16.31 ATOM 2291 O HOH 599 29.834 27.545 68.444 1.00 22.39 ATOM 2292 O HOH 600 37.953 40.975 40.829 1.00 14.27 ATOM 2293 O HOH 601 12.155 45.294 67.909 1.00 17.65 ATOM 2294 O HOH 602 22.482 36.971 50.284 1.00 24.49 ATOM 2295 O HOH 603 23.544 68.425 75.283 1.00 28.58 ATOM 2296 O HOH 604 45.872 62.745 70.934 1.00 20.85 ATOM 2297 O HOH 605 27.938 49.214 42.120 1.00 30.40 ATOM 2298 O HOH 606 27.096 61.728 78.244 1.00 24.23 ATOM 2299 O HOH 607 31.086 37.382 40.546 1.00 19.00 ATOM 2300 O HOH 608 41.624 62.545 78.909 1.00 18.97 ATOM 2301 O HOH 609 41.687 56.553 77.779 1.00 20.00 ATOM 2302 O HOH 610 24.401 57.605 65.060 1.00 18.11 ATOM 2303 O HOH 611 22.321 34.679 80.031 1.00 20.17 ATOM 2304 O HOH 612 50.721 43.533 70.330 1.00 19.94 ATOM 2305 O HOH 613 13.420 52.527 51.343 1.00 25.95 ATOM 2306 O HOH 614 24.279 27.169 60.916 1.00 21.76 ATOM 2307 O HOH 615 34.037 52.439 85.454 1.00 17.26 ATOM 2308 O HOH 616 39.054 65.244 80.148 1.00 24.89 ATOM 2309 O HOH 617 39.054 64.302 51.723 1.00 29.39 ATOM 2310 O HOH 618 43.601 62.259 58.842 1.00 27.04 ATOM 2311 O HOH 619 22.409 56.766 90.280 1.00 33.32 ATOM 2312 O HOH 620 20.846 28.993 74.299 1.00 20.46 ATOM 2313 O HOH 621 17.253 46.648 86.012 1.00 32.49 ATOM 2314 O HOH 622 21.298 51.633 88.129 1.00 31.62 ATOM 2315 O HOH 623 28.632 26.574 61.870 1.00 27.33 ATOM 2316 O HOH 624 48.345 58.417 61.097 1.00 25.77 ATOM 2317 O HOH 625 36.305 67.237 72.635 1.00 20.04 ATOM 2318 O HOH 626 42.598 53.012 75.632 1.00 19.40 ATOM 2319 O HOH 627 20.218 47.782 86.726 1.00 22.94 ATOM 2320 O HOH 628 32.159 63.722 48.806 1.00 23.31 ATOM 2321 O HOH 629 23.413 63.225 51.020 1.00 26.53 ATOM 2322 O HOH 630 29.942 43.073 43.112 1.00 28.69 ATOM 2323 O HOH 631 26.522 26.069 67.811 1.00 29.08 ATOM 2324 O HOH 632 22.688 56.444 82.013 1.00 24.60 ATOM 2325 O HOH 633 52.189 43.104 63.856 1.00 22.68 ATOM 2326 O HOH 634 25.706 64.912 64.257 1.00 22.84 ATOM 2327 O HOH 635 36.511 40.834 83.556 1.00 23.63 ATOM 2328 O HOH 636 31.226 27.212 64.879 1.00 21.79 ATOM 2329 O HOH 637 40.945 34.644 81.702 1.00 23.90 ATOM 2330 O HOH 638 21.448 59.284 81.673 1.00 34.56 ATOM 2331 O HOH 639 49.130 60.035 70.370 1.00 30.49 ATOM 2332 O HOH 640 45.879 54.032 77.176 1.00 28.11 ATOM 2333 O HOH 641 41.217 55.181 84.434 1.00 27.45 ATOM 2334 O HOH 642 15.917 59.351 77.084 1.00 22.78 ATOM 2335 O HOH 643 26.422 58.999 59.868 1.00 26.25 ATOM 2336 O HOH 644 23.973 36.865 54.522 1.00 23.25 ATOM 2337 O HOH 645 23.524 48.998 51.566 1.00 30.36 ATOM 2338 O HOH 646 46.194 61.930 74.996 1.00 35.99 ATOM 2339 O HOH 647 9.547 44.920 75.322 1.00 30.40 ATOM 2340 O HOH 648 40.501 29.426 67.866 1.00 27.54 ATOM 2341 O HOH 649 42.953 47.204 81.751 1.00 28.53 ATOM 2342 O HOH 650 26.628 46.271 47.232 1.00 28.74 ATOM 2343 O HOH 651 41.609 36.542 46.766 1.00 26.30 ATOM 2344 O HOH 652 47.789 62.434 66.963 1.00 22.24 ATOM 2345 O HOH 653 49.409 58.883 57.890 1.00 32.71 ATOM 2346 O HOH 654 17.321 49.855 67.521 1.00 17.23 ATOM 2347 O HOH 655 51.495 46.932 72.085 1.00 20.28 ATOM 2348 O HOH 656 34.466 27.259 73.207 1.00 21.37 ATOM 2349 O HOH 657 38.002 69.000 71.442 1.00 14.96 ATOM 2350 O HOH 658 20.746 31.132 65.541 1.00 23.69 ATOM 2351 O HOH 659 58.157 43.951 58.062 1.00 20.32 ATOM 2352 O HOH 660 38.437 33.849 81.870 1.00 20.83 ATOM 2353 O HOH 661 43.258 34.683 60.615 1.00 17.70 ATOM 2354 O HOH 662 36.377 51.103 84.600 1.00 27.30 ATOM 2355 O HOH 663 25.933 38.583 81.765 1.00 24.70 ATOM 2356 O HOH 664 29.974 47.696 49.284 1.00 24.16 ATOM 2357 O HOH 665 49.678 57.581 72.793 1.00 26.38 ATOM 2358 O HOH 666 50.099 56.413 54.533 1.00 21.01 ATOM 2359 O HOH 667 52.662 42.022 61.588 1.00 28.15 ATOM 2360 O HOH 668 20.130 54.995 81.261 1.00 24.64 ATOM 2361 O HOH 669 46.100 40.982 44.473 1.00 25.43 ATOM 2362 O HOH 670 47.498 47.532 45.696 1.00 27.31 ATOM 2363 O HOH 671 32.535 33.305 43.257 1.00 27.22 ATOM 2364 O HOH 672 43.715 31.852 63.188 1.00 19.52 ATOM 2365 O HOH 673 24.492 65.745 55.161 1.00 28.73 ATOM 2366 O HOH 674 27.731 64.219 61.902 1.00 29.97 ATOM 2367 O HOH 675 44.865 49.755 80.491 1.00 26.39 ATOM 2368 O HOH 676 37.157 68.382 83.515 1.00 28.68 ATOM 2369 O HOH 677 30.154 55.040 89.681 1.00 29.35 ATOM 2370 O HOH 678 30.684 39.377 42.310 1.00 17.22 ATOM 2371 O HOH 679 18.954 28.710 77.300 1.00 34.29 ATOM 2372 O HOH 680 36.128 60.169 43.709 1.00 32.96 ATOM 2373 O HOH 681 41.469 52.484 78.099 1.00 23.04 ATOM 2374 O HOH 682 26.597 36.390 48.638 1.00 26.34 ATOM 2375 O HOH 683 50.624 46.042 56.343 1.00 27.15 ATOM 2376 O HOH 684 32.352 60.908 62.085 1.00 29.37 ATOM 2377 O HOH 685 36.543 42.286 39.079 1.00 36.28 ATOM 2378 O HOH 686 13.775 50.845 82.171 1.00 28.05 ATOM 2379 O HOH 687 47.886 43.395 52.513 1.00 28.22 ATOM 2380 O HOH 688 50.808 53.317 53.903 1.00 33.82 ATOM 2381 O HOH 689 33.470 54.665 86.847 1.00 17.58 ATOM 2382 O HOH 690 19.330 58.463 73.532 1.00 17.09 ATOM 2383 O HOH 691 51.990 49.111 66.439 1.00 25.06 ATOM 2384 O HOH 692 55.576 56.592 60.334 1.00 24.70 ATOM 2385 O HOH 693 50.867 41.843 47.444 1.00 32.36 ATOM 2386 O HOH 694 28.359 36.216 43.792 1.00 27.71 ATOM 2387 O HOH 695 30.229 40.375 82.671 1.00 15.17 ATOM 2388 O HOH 696 34.080 42.336 41.876 1.00 15.17 ATOM 2389 C ACY 244 23.704 53.254 68.309 1.00 20.17 ATOM 2390 O ACY 244 24.283 54.249 68.921 1.00 20.17 ATOM 2391 OXT ACY 244 23.988 52.013 68.413 1.00 20.17 ATOM 2392 CH3 ACY 244 22.577 53.681 67.378 1.00 20.17

[0495] TABLE 5 REMARK coordinates from minimization refinement REMARK refinement resolution: 20.0-2.0 A REMARK starting r = .2565 free_r = .2833 REMARK final   r = .2545 free_r = .2823 REMARK rmsd bonds = .006693 rmsd angles = 1.31286 REMARK wa = 1.49748 REMARK target = mlf cycles = 1 steps = 25 REMARK sg = P2 (1) 2 (1) 2 (1) a = 39.975 b = 76.158 c = 87.228 alpha = 90 beta = 90 gamma = 90 REMARK parameter file 1: CNS_TOPPAR: protein_rep.param REMARK parameter file 2: ../upg.par REMARK parameter file 3: CNS_TOPPAR: ion.param REMARK parameter file 4: CNS_TOPPAR: water_rep.param REMARK parameter file 5: ../lat.par REMARK molecular structure file: generate3.mtf REMARK input coordinates: generate3.pdb REMARK reflection file = ../../deoxyse.cv REMARK ncs = none REMARK B-correction resolution: 6.0-2.0 REMARK initial B-factor correction applied to fobs: REMARK  B11 = 1.331 B22 = 2.292 B33 = −3.623 REMARK  B12 = .000 B13 = .000 B23 = .000 REMARK B-factor correction applied to coordinate array B: −.107 REMARK bulk solvent: density level = .364834 e/A{circumflex over ( )}3, B-factor = 28.3776 A{circumflex over ( )}2 REMARK reflections with |Fobs|/sigma_F < 0.0 rejected REMARK reflections with |Fobs| > 10000 * rms (Fobs) rejected REMARK theoretical total number of refl. in resol. range: 18599 (>100.0%) REMARK number of unobserved reflections (no entry or |F| = 0):  374 (>2.0%) REMARK number of reflections rejected:   0 (.0%) REMARK total number of reflections used: 18225 (>98.0%) REMARK number of reflections in working set: 17339 (93.2%) REMARK number of reflections in test set:  886 (>4.8%) CRYST1  39.975  76.158  87.228  90.00  90.00  90.00 P 21 21 21 REMARK FILENAME = “minimize3.pdb” REMARK DATE: 7-Jun-00  00:41:57   created by user: karina REMARK VERSION: 1.0 ATOM 1 CB MSE 1 48.137 46.257 65.175 1.00 15.20 DIC ATOM 2 CG MSE 1 47.648 47.190 64.082 1.00 16.41 DIC ATOM 3 SE MSE 1 46.777 48.813 64.794 1.00 17.84 DIC ATOM 4 CE MSE 1 48.349 49.605 65.593 1.00 17.32 DIC ATOM 5 C MSE 1 47.761 44.130 63.891 1.00 12.29 DIC ATOM 6 O MSE 1 47.811 44.149 62.665 1.00 12.03 DIC ATOM 7 N MSE 1 50.002 45.161 63.937 1.00 12.69 DIC ATOM 8 CA MSE 1 48.762 44.924 64.719 1.00 12.79 DIC ATOM 9 N ASP 2 46.865 43.424 64.570 1.00 11.18 DIC ATOM 10 CA ASP 2 45.852 42.621 63.902 1.00 11.07 DIC ATOM 11 CB ASP 2 45.779 41.223 64.516 1.00 11.12 DIC ATOM 12 CG ASP 2 47.054 40.435 64.305 1.00 12.17 DIC ATOM 13 OD1 ASP 2 47.948 40.480 65.180 1.00 11.27 DIC ATOM 14 OD2 ASP 2 47.164 39.783 63.247 1.00 12.68 DIC ATOM 15 C ASP 2 44.494 43.289 63.985 1.00 10.71 DIC ATOM 16 O ASP 2 43.971 43.534 65.072 1.00 10.39 DIC ATOM 17 N ILE 3 43.946 43.590 62.813 1.00 9.90 DIC ATOM 18 CA ILE 3 42.650 44.245 62.675 1.00 9.22 DIC ATOM 19 CB ILE 3 42.716 45.381 61.627 1.00 9.23 DIC ATOM 20 CG2 ILE 3 41.353 46.043 61.480 1.00 6.69 DIC ATOM 21 CG1 ILE 3 43.799 46.392 62.019 1.00 8.74 DIC ATOM 22 CD ILE 3 43.544 47.108 63.340 1.00 10.46 DIC ATOM 23 C ILE 3 41.649 43.216 62.186 1.00 9.22 DIC ATOM 24 O ILE 3 41.974 42.392 61.330 1.00 8.87 DIC ATOM 25 N VAL 4 40.443 43.262 62.738 1.00 9.68 DIC ATOM 26 CA VAL 4 39.383 42.346 62.343 1.00 9.18 DIC ATOM 27 CB VAL 4 38.861 41.512 63.519 1.00 9.44 DIC ATOM 28 CG1 VAL 4 37.758 40.566 63.024 1.00 9.88 DIC ATOM 29 CG2 VAL 4 39.994 40.741 64.157 1.00 9.29 DIC ATOM 30 C VAL 4 38.198 43.127 61.807 1.00 9.80 DIC ATOM 31 O VAL 4 37.805 44.137 62.381 1.00 8.97 DIC ATOM 32 N PHE 5 37.653 42.651 60.693 1.00 9.50 DIC ATOM 33 CA PHE 5 36.477 43.241 60.060 1.00 9.57 DIC ATOM 34 CB PHE 5 36.823 43.854 58.694 1.00 9.78 DIC ATOM 35 CG PHE 5 37.479 45.205 58.763 1.00 8.54 DIC ATOM 36 CD1 PHE 5 36.784 46.308 59.248 1.00 7.97 DIC ATOM 37 CD2 PHE 5 38.772 45.385 58.283 1.00 9.19 DIC ATOM 38 CE1 PHE 5 37.368 47.577 59.246 1.00 8.53 DIC ATOM 39 CE2 PHE 5 39.366 46.645 58.275 1.00 9.07 DIC ATOM 40 CZ PHE 5 38.661 47.744 58.757 1.00 9.04 DIC ATOM 41 C PHE 5 35.544 42.052 59.818 1.00 9.75 DIC ATOM 42 O PHE 5 35.985 40.896 59.803 1.00 8.48 DIC ATOM 43 N ALA 6 34.265 42.338 59.638 1.00 8.31 DIC ATOM 44 CA ALA 6 33.273 41.316 59.345 1.00 9.26 DIC ATOM 45 CB ALA 6 32.416 41.019 60.572 1.00 9.18 DIC ATOM 46 C ALA 6 32.424 41.941 58.252 1.00 9.59 DIC ATOM 47 O ALA 6 31.983 43.077 58.388 1.00 9.30 DIC ATOM 48 N ALA 7 32.195 41.218 57.165 1.00 9.68 DIC ATOM 49 CA ALA 7 31.385 41.777 56.088 1.00 9.55 DIC ATOM 50 CB ALA 7 32.242 42.714 55.237 1.00 10.43 DIC ATOM 51 C ALA 7 30.784 40.703 55.205 1.00 10.26 DIC ATOM 52 O ALA 7 31.358 39.628 55.069 1.00 9.81 DIC ATOM 53 N ASP 8 29.614 40.982 54.630 1.00 10.79 DIC ATOM 54 CA ASP 8 29.008 40.048 53.693 1.00 10.98 DIC ATOM 55 CB ASP 8 27.481 39.986 53.822 1.00 11.13 DIC ATOM 56 CG ASP 8 26.852 41.337 54.092 1.00 10.25 DIC ATOM 57 OD1 ASP 8 27.419 42.365 53.676 1.00 8.93 DIC ATOM 58 OD2 ASP 8 25.768 41.361 54.719 1.00 11.96 DIC ATOM 59 C ASP 8 29.399 40.620 52.340 1.00 12.11 DIC ATOM 60 O ASP 8 30.143 41.596 52.281 1.00 11.30 DIC ATOM 61 N ASP 9 28.903 40.042 51.255 1.00 12.32 DIC ATOM 62 CA ASP 9 29.269 40.534 49.931 1.00 13.23 DIC ATOM 63 CB ASP 9 28.701 39.607 48.852 1.00 14.44 DIC ATOM 64 CG ASP 9 29.286 39.890 47.486 1.00 14.65 DIC ATOM 65 OD1 ASP 9 30.516 39.787 47.335 1.00 13.72 DIC ATOM 66 OD2 ASP 9 28.520 40.222 46.567 1.00 17.00 DIC ATOM 67 C ASP 9 28.817 41.977 49.674 1.00 13.55 DIC ATOM 68 O ASP 9 29.500 42.737 48.984 1.00 12.70 DIC ATOM 69 N ASN 10 27.671 42.349 50.237 1.00 13.42 DIC ATOM 70 CA ASN 10 27.122 43.689 50.068 1.00 13.87 DIC ATOM 71 CB ASN 10 25.804 43.814 50.836 1.00 14.04 DIC ATOM 72 CG ASN 10 25.148 45.171 50.650 1.00 15.16 DIC ATOM 73 OD1 ASN 10 24.977 45.634 49.523 1.00 14.38 DIC ATOM 74 ND2 ASN 10 24.767 45.810 51.754 1.00 13.92 DIC ATOM 75 C ASN 10 28.074 44.794 50.527 1.00 13.56 DIC ATOM 76 O ASN 10 28.076 45.900 49.965 1.00 13.16 DIC ATOM 77 N TYR 11 28.879 44.492 51.541 1.00 12.92 DIC ATOM 78 CA TYR 11 29.821 45.460 52.091 1.00 13.06 DIC ATOM 79 CB TYR 11 29.733 45.440 53.616 1.00 13.83 DIC ATOM 80 CG TYR 11 28.756 46.430 54.192 1.00 14.83 DIC ATOM 81 CD1 TYR 11 27.652 46.865 53.459 1.00 14.49 DIC ATOM 82 CE1 TYR 11 26.758 47.782 53.995 1.00 15.54 DIC ATOM 83 CD2 TYR 11 28.934 46.935 55.480 1.00 15.47 DIC ATOM 84 CE2 TYR 11 28.044 47.849 56.021 1.00 16.13 DIC ATOM 85 CZ TYR 11 26.962 48.268 55.277 1.00 15.85 DIC ATOM 86 OH TYR 11 26.082 49.171 55.822 1.00 17.10 DIC ATOM 87 C TYR 11 31.278 45.291 51.677 1.00 13.35 DIC ATOM 88 O TYR 11 32.156 45.945 52.246 1.00 12.67 DIC ATOM 89 N ALA 12 31.540 44.436 50.689 1.00 12.77 DIC ATOM 90 CA ALA 12 32.905 44.196 50.226 1.00 11.93 DIC ATOM 91 CB ALA 12 32.898 43.176 49.085 1.00 12.43 DIC ATOM 92 C ALA 12 33.646 45.465 49.786 1.00 12.10 DIC ATOM 93 O ALA 12 34.812 45.659 50.131 1.00 9.34 DIC ATOM 94 N ALA 13 32.981 46.321 49.014 1.00 11.40 DIC ATOM 95 CA ALA 13 33.614 47.552 48.548 1.00 11.49 DIC ATOM 96 CB ALA 13 32.711 48.259 47.525 1.00 12.59 DIC ATOM 97 C ALA 13 33.935 48.486 49.719 1.00 11.12 DIC ATOM 98 O ALA 13 35.028 49.062 49.786 1.00 10.82 DIC ATOM 99 N TYR 14 32.988 48.624 50.643 1.00 10.01 DIC ATOM 100 CA TYR 14 33.169 49.479 51.812 1.00 10.22 DIC ATOM 101 CB TYR 14 31.869 49.535 52.623 1.00 10.13 DIC ATOM 102 CG TYR 14 30.670 49.883 51.775 1.00 11.37 DIC ATOM 103 CD1 TYR 14 30.798 50.752 50.692 1.00 11.46 DIC ATOM 104 CE1 TYR 14 29.709 51.098 49.913 1.00 12.49 DIC ATOM 105 CD2 TYR 14 29.406 49.363 52.061 1.00 11.77 DIC ATOM 106 CE2 TYR 14 28.301 49.708 51.288 1.00 12.94 DIC ATOM 107 CZ TYR 14 28.464 50.581 50.211 1.00 13.37 DIC ATOM 108 OH TYR 14 27.387 50.969 49.445 1.00 13.68 DIC ATOM 109 C TYR 14 34.320 48.993 52.692 1.00 10.01 DIC ATOM 110 O TYR 14 35.101 49.796 53.209 1.00 10.44 DIC ATOM 111 N LEU 15 34.402 47.677 52.864 1.00 9.93 DIC ATOM 112 CA LEU 15 35.454 47.043 53.649 1.00 10.44 DIC ATOM 113 CB LEU 15 35.311 45.523 53.558 1.00 10.41 DIC ATOM 114 CG LEU 15 36.559 44.670 53.803 1.00 11.91 DIC ATOM 115 CD1 LEU 15 36.951 44.732 55.262 1.00 12.15 DIC ATOM 116 CD2 LEU 15 36.282 43.228 53.380 1.00 10.34 DIC ATOM 117 C LEU 15 36.822 47.451 53.097 1.00 9.78 DIC ATOM 118 O LEU 15 37.767 47.689 53.852 1.00 10.03 DIC ATOM 119 N CYS 16 36.917 47.505 51.771 1.00 9.90 DIC ATOM 120 CA CYS 16 38.160 47.878 51.111 1.00 9.59 DIC ATOM 121 CB CYS 16 38.005 47.761 49.590 1.00 9.35 DIC ATOM 122 SG CYS 16 39.528 48.155 48.711 1.00 10.55 DIC ATOM 123 C CYS 16 38.574 49.301 51.483 1.00 9.71 DIC ATOM 124 O CYS 16 39.737 49.564 51.793 1.00 10.85 DIC ATOM 125 N VAL 17 37.618 50.219 51.452 1.00 9.93 DIC ATOM 126 CA VAL 17 37.891 51.611 51.805 1.00 10.54 DIC ATOM 127 CB VAL 17 36.663 52.502 51.509 1.00 9.19 DIC ATOM 128 CG1 VAL 17 36.853 53.889 52.088 1.00 9.35 DIC ATOM 129 CG2 VAL 17 36.459 52.596 49.993 1.00 10.21 DIC ATOM 130 C VAL 17 38.277 51.730 53.281 1.00 11.16 DIC ATOM 131 O VAL 17 39.214 52.445 53.625 1.00 12.58 DIC ATOM 132 N ALA 18 37.562 51.031 54.154 1.00 11.08 DIC ATOM 133 CA ALA 18 37.877 51.094 55.580 1.00 10.23 DIC ATOM 134 CB ALA 18 36.838 50.319 56.390 1.00 9.79 DIC ATOM 135 C ALA 18 39.267 50.515 55.830 1.00 10.26 DIC ATOM 136 O ALA 18 40.059 51.075 56.598 1.00 9.16 DIC ATOM 137 N ALA 19 39.554 49.387 55.187 1.00 10.33 DIC ATOM 138 CA ALA 19 40.843 48.729 55.343 1.00 11.10 DIC ATOM 139 CB ALA 19 40.883 47.450 54.519 1.00 12.50 DIC ATOM 140 C ALA 19 41.955 49.672 54.910 1.00 12.35 DIC ATOM 141 O ALA 19 42.945 49.839 55.620 1.00 11.18 DIC ATOM 142 N LYS 20 41.786 50.307 53.755 1.00 12.66 DIC ATOM 143 CA LYS 20 42.812 51.227 53.277 1.00 13.17 DIC ATOM 144 CB LYS 20 42.485 51.723 51.872 1.00 14.36 DIC ATOM 145 CG LYS 20 43.592 52.576 51.284 1.00 18.06 DIC ATOM 146 CD LYS 20 43.350 52.878 49.815 1.00 21.04 DIC ATOM 147 CE LYS 20 44.518 53.666 49.229 1.00 22.73 DIC ATOM 148 NZ LYS 20 44.283 54.010 47.797 1.00 23.84 DIC ATOM 149 C LYS 20 42.994 52.410 54.227 1.00 12.86 DIC ATOM 150 O LYS 20 44.114 52.877 54.426 1.00 11.70 DIC ATOM 151 N SER 21 41.909 52.893 54.830 1.00 12.92 DIC ATOM 152 CA SER 21 42.049 54.014 55.759 1.00 13.27 DIC ATOM 153 CB SER 21 40.684 54.476 56.298 1.00 13.74 DIC ATOM 154 OG SER 21 40.217 53.672 57.370 1.00 13.06 DIC ATOM 155 C SER 21 42.964 53.580 56.904 1.00 12.88 DIC ATOM 156 O SER 21 43.782 54.360 57.383 1.00 13.01 DIC ATOM 157 N VAL 22 42.845 52.327 57.332 1.00 13.22 DIC ATOM 158 CA VAL 22 43.698 51.825 58.410 1.00 12.36 DIC ATOM 159 CB VAL 22 43.308 50.398 58.836 1.00 12.30 DIC ATOM 160 CG1 VAL 22 44.288 49.892 59.872 1.00 11.72 DIC ATOM 161 CG2 VAL 22 41.887 50.383 59.389 1.00 11.48 DIC ATOM 162 C VAL 22 45.164 51.799 57.979 1.00 12.37 DIC ATOM 163 O VAL 22 46.059 52.159 58.749 1.00 11.98 DIC ATOM 164 N GLU 23 45.420 51.364 56.751 1.00 12.92 DIC ATOM 165 CA GLU 23 46.800 51.317 56.276 1.00 13.21 DIC ATOM 166 CB GLU 23 46.890 50.655 54.897 1.00 13.48 DIC ATOM 167 CG GLU 23 46.489 49.186 54.863 1.00 14.09 DIC ATOM 168 CD GLU 23 46.831 48.546 53.536 1.00 14.75 DIC ATOM 169 OE1 GLU 23 46.676 49.224 52.503 1.00 14.77 DIC ATOM 170 OE2 GLU 23 47.247 47.369 53.519 1.00 14.64 DIC ATOM 171 C GLU 23 47.376 52.724 56.193 1.00 13.14 DIC ATOM 172 O GLU 23 48.504 52.961 56.615 1.00 13.52 DIC ATOM 173 N ALA 24 46.591 53.653 55.649 1.00 11.95 DIC ATOM 174 CA ALA 24 47.030 55.032 55.501 1.00 12.18 DIC ATOM 175 CB ALA 24 45.916 55.881 54.857 1.00 13.20 DIC ATOM 176 C ALA 24 47.433 55.636 56.833 1.00 11.58 DIC ATOM 177 O ALA 24 48.382 56.422 56.905 1.00 10.67 DIC ATOM 178 N ALA 25 46.722 55.259 57.891 1.00 11.32 DIC ATOM 179 CA ALA 25 46.994 55.784 59.225 1.00 11.21 DIC ATOM 180 CB ALA 25 45.745 55.648 60.096 1.00 10.62 DIC ATOM 181 C ALA 25 48.199 55.160 59.939 1.00 11.67 DIC ATOM 182 O ALA 25 48.613 55.651 60.985 1.00 11.24 DIC ATOM 183 N HIS 26 48.763 54.088 59.393 1.00 11.30 DIC ATOM 184 CA HIS 26 49.926 53.459 60.027 1.00 12.66 DIC ATOM 185 CB HIS 26 49.529 52.171 60.761 1.00 12.73 DIC ATOM 186 CG HIS 26 48.360 52.331 61.682 1.00 14.25 DIC ATOM 187 CD2 HIS 26 48.296 52.451 63.030 1.00 13.73 DIC ATOM 188 ND1 HIS 26 47.058 52.385 61.229 1.00 13.15 DIC ATOM 189 CE1 HIS 26 46.244 52.529 62.258 1.00 13.73 DIC ATOM 190 NE2 HIS 26 46.970 52.571 63.362 1.00 14.21 DIC ATOM 191 C HIS 26 50.968 53.126 58.965 1.00 12.72 DIC ATOM 192 O HIS 26 51.201 51.956 58.654 1.00 12.84 DIC ATOM 193 N PRO 27 51.616 54.155 58.402 1.00 13.48 DIC ATOM 194 CD PRO 27 51.482 55.586 58.732 1.00 14.47 DIC ATOM 195 CA PRO 27 52.628 53.949 57.369 1.00 14.03 DIC ATOM 196 CB PRO 27 53.064 55.377 57.015 1.00 14.64 DIC ATOM 197 CG PRO 27 52.802 56.148 58.271 1.00 15.02 DIC ATOM 198 C PRO 27 53.800 53.040 57.730 1.00 13.73 DIC ATOM 199 O PRO 27 54.418 52.447 56.842 1.00 14.16 DIC ATOM 200 N ASP 28 54.119 52.912 59.013 1.00 13.19 DIC ATOM 201 CA ASP 28 55.240 52.044 59.368 1.00 13.54 DIC ATOM 202 CB ASP 28 56.407 52.855 59.934 1.00 14.01 DIC ATOM 203 CG ASP 28 57.687 52.033 60.027 1.00 12.49 DIC ATOM 204 OD1 ASP 28 57.987 51.294 59.066 1.00 13.79 DIC ATOM 205 OD2 ASP 28 58.390 52.123 61.047 1.00 11.67 DIC ATOM 206 C ASP 28 54.883 50.930 60.335 1.00 14.24 DIC ATOM 207 O ASP 28 55.706 50.504 61.146 1.00 13.51 DIC ATOM 208 N THR 29 53.651 50.450 60.242 1.00 14.30 DIC ATOM 209 CA THR 29 53.219 49.367 61.102 1.00 15.03 DIC ATOM 210 CB THR 29 52.156 49.818 62.104 1.00 13.26 DIC ATOM 211 OG1 THR 29 52.632 50.956 62.828 1.00 12.77 DIC ATOM 212 CG2 THR 29 51.865 48.694 63.090 1.00 13.03 DIC ATOM 213 C THR 29 52.636 48.266 60.243 1.00 15.57 DIC ATOM 214 O THR 29 51.882 48.528 59.305 1.00 14.98 DIC ATOM 215 N GLU 30 53.012 47.034 60.554 1.00 16.16 DIC ATOM 216 CA GLU 30 52.520 45.874 59.825 1.00 17.32 DIC ATOM 217 CB GLU 30 53.287 44.630 60.281 1.00 19.02 DIC ATOM 218 CG GLU 30 53.694 43.659 59.178 1.00 23.03 DIC ATOM 219 CD GLU 30 54.316 44.344 57.969 1.00 23.93 DIC ATOM 220 OE1 GLU 30 53.564 44.698 57.039 1.00 24.55 DIC ATOM 221 OE2 GLU 30 55.549 44.537 57.947 1.00 24.76 DIC ATOM 222 C GLU 30 51.046 45.750 60.185 1.00 16.48 DIC ATOM 223 O GLU 30 50.701 45.675 61.368 1.00 16.29 DIC ATOM 224 N ILE 31 50.174 45.760 59.181 1.00 15.30 DIC ATOM 225 CA ILE 31 48.743 45.628 59.436 1.00 15.17 DIC ATOM 226 CB ILE 31 47.905 46.770 58.778 1.00 14.27 DIC ATOM 227 CG2 ILE 31 46.420 46.573 59.106 1.00 14.26 DIC ATOM 228 CG1 ILE 31 48.368 48.140 59.277 1.00 13.70 DIC ATOM 229 CD ILE 31 48.085 48.397 60.740 1.00 12.11 DIC ATOM 230 C ILE 31 48.245 44.305 58.868 1.00 14.65 DIC ATOM 231 O ILE 31 48.185 44.127 57.650 1.00 14.91 DIC ATOM 232 N ARG 32 47.891 43.384 59.757 1.00 13.99 DIC ATOM 233 CA ARG 32 47.384 42.087 59.349 1.00 13.79 DIC ATOM 234 CB ARG 32 47.983 40.982 60.225 1.00 15.26 DIC ATOM 235 CG ARG 32 49.510 40.934 60.177 1.00 18.70 DIC ATOM 236 CD ARG 32 50.067 39.639 60.752 1.00 21.47 DIC ATOM 237 NE ARG 32 49.766 39.471 62.173 1.00 24.86 DIC ATOM 238 CZ ARG 32 50.180 38.439 62.905 1.00 27.54 DIC ATOM 239 NH1 ARG 32 50.916 37.483 62.346 1.00 28.88 DIC ATOM 240 NH2 ARG 32 49.861 38.360 64.196 1.00 27.69 DIC ATOM 241 C ARG 32 45.867 42.107 59.478 1.00 13.24 DIC ATOM 242 O ARG 32 45.330 42.234 60.578 1.00 11.50 DIC ATOM 243 N PHE 33 45.185 41.997 58.341 1.00 12.52 DIC ATOM 244 CA PHE 33 43.730 42.009 58.301 1.00 11.78 DIC ATOM 245 CB PHE 33 43.246 42.686 57.010 1.00 10.75 DIC ATOM 246 CG PHE 33 43.502 44.171 56.950 1.00 9.65 DIC ATOM 247 CD1 PHE 33 42.777 45.054 57.748 1.00 9.25 DIC ATOM 248 CD2 PHE 33 44.414 44.693 56.038 1.00 10.53 DIC ATOM 249 CE1 PHE 33 42.953 46.436 57.627 1.00 9.15 DIC ATOM 250 CE2 PHE 33 44.600 46.077 55.908 1.00 9.49 DIC ATOM 251 CZ PHE 33 43.864 46.944 56.703 1.00 9.68 DIC ATOM 252 C PHE 33 43.134 40.597 58.365 1.00 11.96 DIC ATOM 253 O PHE 33 43.565 39.697 57.639 1.00 12.74 DIC ATOM 254 N HIS 34 42.145 40.420 59.238 1.00 11.46 DIC ATOM 255 CA HIS 34 41.431 39.149 59.403 1.00 11.17 DIC ATOM 256 CB HIS 34 41.523 38.659 60.850 1.00 11.57 DIC ATOM 257 CG HIS 34 42.919 38.593 61.384 1.00 12.66 DIC ATOM 258 CD2 HIS 34 43.704 39.544 61.942 1.00 13.37 DIC ATOM 259 ND1 HIS 34 43.667 37.437 61.370 1.00 13.22 DIC ATOM 260 CE1 HIS 34 44.854 37.677 61.899 1.00 13.27 DIC ATOM 261 NE2 HIS 34 44.903 38.947 62.255 1.00 14.11 DIC ATOM 262 C HIS 34 39.971 39.480 59.091 1.00 11.20 DIC ATOM 263 O HIS 34 39.336 40.217 59.830 1.00 9.79 DIC ATOM 264 N VAL 35 39.428 38.944 58.010 1.00 10.16 DIC ATOM 265 CA VAL 35 38.050 39.266 57.679 1.00 10.38 DIC ATOM 266 CB VAL 35 37.945 39.733 56.208 1.00 11.51 DIC ATOM 267 CG1 VAL 35 36.512 40.077 55.867 1.00 11.42 DIC ATOM 268 CG2 VAL 35 38.847 40.945 55.985 1.00 12.17 DIC ATOM 269 C VAL 35 37.072 38.126 57.929 1.00 10.51 DIC ATOM 270 O VAL 35 37.240 37.017 57.408 1.00 9.02 DIC ATOM 271 N LEU 36 36.060 38.397 58.754 1.00 10.05 DIC ATOM 272 CA LEU 36 35.027 37.412 59.044 1.00 10.98 DIC ATOM 273 CB LEU 36 34.282 37.766 60.341 1.00 11.52 DIC ATOM 274 CG LEU 36 35.176 37.835 61.592 1.00 12.34 DIC ATOM 275 CD1 LEU 36 34.319 37.965 62.858 1.00 13.53 DIC ATOM 276 CD2 LEU 36 36.035 36.574 61.679 1.00 13.20 DIC ATOM 277 C LEU 36 34.123 37.527 57.821 1.00 11.61 DIC ATOM 278 O LEU 36 33.275 38.409 57.728 1.00 10.93 DIC ATOM 279 N ASP 37 34.352 36.620 56.881 1.00 12.50 DIC ATOM 280 CA ASP 37 33.678 36.580 55.591 1.00 13.19 DIC ATOM 281 CB ASP 37 34.660 35.981 54.580 1.00 13.28 DIC ATOM 282 CG ASP 37 34.090 35.878 53.189 1.00 13.48 DIC ATOM 283 OD1 ASP 37 32.903 36.212 52.997 1.00 14.14 DIC ATOM 284 OD2 ASP 37 34.843 35.456 52.290 1.00 13.50 DIC ATOM 285 C ASP 37 32.369 35.803 55.588 1.00 14.68 DIC ATOM 286 O ASP 37 32.363 34.569 55.634 1.00 14.18 DIC ATOM 287 N ALA 38 31.258 36.526 55.511 1.00 14.79 DIC ATOM 288 CA ALA 38 29.954 35.884 55.521 1.00 15.72 DIC ATOM 289 CB ALA 38 28.983 36.689 56.390 1.00 16.90 DIC ATOM 290 C ALA 38 29.362 35.669 54.132 1.00 15.90 DIC ATOM 291 O ALA 38 28.143 35.600 53.978 1.00 17.34 DIC ATOM 292 N GLY 39 30.213 35.557 53.120 1.00 15.36 DIC ATOM 293 CA GLY 39 29.698 35.321 51.786 1.00 13.98 DIC ATOM 294 C GLY 39 30.208 36.249 50.706 1.00 12.66 DIC ATOM 295 O GLY 39 29.534 36.454 49.701 1.00 13.26 DIC ATOM 296 N ILE 40 31.395 36.805 50.901 1.00 11.81 DIC ATOM 297 CA ILE 40 31.985 37.695 49.909 1.00 12.00 DIC ATOM 298 CB ILE 40 33.220 38.417 50.493 1.00 11.76 DIC ATOM 299 CG2 ILE 40 33.764 39.419 49.488 1.00 12.77 DIC ATOM 300 CG1 ILE 40 32.815 39.178 51.761 1.00 10.15 DIC ATOM 301 CD ILE 40 33.981 39.741 52.549 1.00 10.52 DIC ATOM 302 C ILE 40 32.389 36.857 48.688 1.00 12.84 DIC ATOM 303 O ILE 40 32.958 35.772 48.828 1.00 12.10 DIC ATOM 304 N SER 41 32.078 37.350 47.491 1.00 13.34 DIC ATOM 305 CA SER 41 32.410 36.629 46.265 1.00 13.44 DIC ATOM 306 CB SER 41 31.778 37.311 45.043 1.00 12.76 DIC ATOM 307 OG SER 41 32.427 38.536 44.747 1.00 12.89 DIC ATOM 308 C SER 41 33.909 36.552 46.055 1.00 14.12 DIC ATOM 309 O SER 41 34.662 37.369 46.583 1.00 14.41 DIC ATOM 310 N GLU 42 34.336 35.570 45.267 1.00 15.57 DIC ATOM 311 CA GLU 42 35.749 35.401 44.968 1.00 16.08 DIC ATOM 312 CB GLU 42 35.967 34.183 44.060 1.00 17.55 DIC ATOM 313 CG GLU 42 37.424 33.922 43.704 1.00 19.96 DIC ATOM 314 CD GLU 42 37.961 34.853 42.631 1.00 21.69 DIC ATOM 315 OE1 GLU 42 39.199 35.047 42.572 1.00 23.34 DIC ATOM 316 OE2 GLU 42 37.153 35.382 41.835 1.00 22.79 DIC ATOM 317 C GLU 42 36.229 36.660 44.265 1.00 15.85 DIC ATOM 318 O GLU 42 37.332 37.137 44.511 1.00 15.67 DIC ATOM 319 N ALA 43 35.385 37.198 43.393 1.00 14.84 DIC ATOM 320 CA ALA 43 35.725 38.399 42.654 1.00 15.14 DIC ATOM 321 CB ALA 43 34.635 38.710 41.622 1.00 15.42 DIC ATOM 322 C ALA 43 35.907 39.579 43.600 1.00 14.89 DIC ATOM 323 O ALA 43 36.821 40.381 43.430 1.00 14.31 DIC ATOM 324 N ASN 44 35.048 39.683 44.610 1.00 15.08 DIC ATOM 325 CA ASN 44 35.163 40.794 45.550 1.00 14.76 DIC ATOM 326 CB ASN 44 33.847 41.008 46.304 1.00 14.30 DIC ATOM 327 CG ASN 44 32.817 41.746 45.464 1.00 15.33 DIC ATOM 328 OD1 ASN 44 33.167 42.625 44.674 1.00 14.17 DIC ATOM 329 ND2 ASN 44 31.543 41.406 45.637 1.00 15.84 DIC ATOM 330 C ASN 44 36.324 40.661 46.529 1.00 14.57 DIC ATOM 331 O ASN 44 36.852 41.666 47.005 1.00 14.31 DIC ATOM 332 N ARG 45 36.732 39.431 46.828 1.00 14.77 DIC ATOM 333 CA ARG 45 37.853 39.229 47.739 1.00 15.32 DIC ATOM 334 CB ARG 45 37.926 37.771 48.205 1.00 16.87 DIC ATOM 335 CG ARG 45 36.589 37.242 48.689 1.00 20.54 DIC ATOM 336 CD ARG 45 36.710 36.377 49.924 1.00 24.39 DIC ATOM 337 NE ARG 45 37.571 35.215 49.725 1.00 27.75 DIC ATOM 338 CZ ARG 45 37.704 34.225 50.608 1.00 29.60 DIC ATOM 339 NH1 ARG 45 37.028 34.247 51.752 1.00 30.56 DIC ATOM 340 NH2 ARG 45 38.526 33.216 50.353 1.00 30.76 DIC ATOM 341 C ARG 45 39.141 39.608 47.020 1.00 15.22 DIC ATOM 342 O ARG 45 40.002 40.277 47.590 1.00 14.16 DIC ATOM 343 N ALA 46 39.265 39.194 45.761 1.00 14.15 DIC ATOM 344 CA ALA 46 40.458 39.515 44.983 1.00 14.85 DIC ATOM 345 CB ALA 46 40.395 38.840 43.610 1.00 15.30 DIC ATOM 346 C ALA 46 40.545 41.029 44.823 1.00 14.64 DIC ATOM 347 O ALA 46 41.623 41.616 44.910 1.00 15.26 DIC ATOM 348 N ALA 47 39.397 41.662 44.600 1.00 14.80 DIC ATOM 349 CA ALA 47 39.348 43.112 44.430 1.00 14.02 DIC ATOM 350 CB ALA 47 37.938 43.536 44.039 1.00 15.12 DIC ATOM 351 C ALA 47 39.795 43.857 45.693 1.00 13.42 DIC ATOM 352 O ALA 47 40.562 44.823 45.618 1.00 12.41 DIC ATOM 353 N VAL 48 39.316 43.415 46.853 1.00 13.25 DIC ATOM 354 CA VAL 48 39.694 44.052 48.111 1.00 12.62 DIC ATOM 355 CB VAL 48 38.922 43.445 49.305 1.00 11.98 DIC ATOM 356 CG1 VAL 48 39.458 43.992 50.609 1.00 10.86 DIC ATOM 357 CG2 VAL 48 37.460 43.786 49.193 1.00 11.68 DIC ATOM 358 C VAL 48 41.192 43.891 48.350 1.00 12.98 DIC ATOM 359 O VAL 48 41.884 44.855 48.682 1.00 12.57 DIC ATOM 360 N ALA 49 41.692 42.672 48.168 1.00 13.13 DIC ATOM 361 CA ALA 49 43.102 42.386 48.374 1.00 14.18 DIC ATOM 362 CB ALA 49 43.355 40.892 48.245 1.00 13.51 DIC ATOM 363 C ALA 49 43.983 43.145 47.397 1.00 14.36 DIC ATOM 364 O ALA 49 45.072 43.601 47.752 1.00 15.03 DIC ATOM 365 N ALA 50 43.519 43.274 46.162 1.00 15.04 DIC ATOM 366 CA ALA 50 44.290 43.979 45.142 1.00 15.89 DIC ATOM 367 CB ALA 50 43.582 43.882 43.792 1.00 16.15 DIC ATOM 368 C ALA 50 44.530 45.443 45.492 1.00 16.46 DIC ATOM 369 O ALA 50 45.515 46.039 45.052 1.00 17.84 DIC ATOM 370 N ASN 51 43.631 46.029 46.277 1.00 16.90 DIC ATOM 371 CA ASN 51 43.758 47.432 46.661 1.00 17.24 DIC ATOM 372 CB ASN 51 42.379 48.060 46.826 1.00 17.14 DIC ATOM 373 CG ASN 51 41.709 48.355 45.507 1.00 16.69 DIC ATOM 374 OD1 ASN 51 42.190 49.172 44.729 1.00 18.27 DIC ATOM 375 ND2 ASN 51 40.584 47.700 45.253 1.00 16.79 DIC ATOM 376 C ASN 51 44.545 47.667 47.942 1.00 18.59 DIC ATOM 377 O ASN 51 44.784 48.815 48.324 1.00 17.91 DIC ATOM 378 N LEU 52 44.946 46.595 48.613 1.00 19.74 DIC ATOM 379 CA LEU 52 45.689 46.750 49.860 1.00 21.37 DIC ATOM 380 CB LEU 52 45.316 45.636 50.834 1.00 20.31 DIC ATOM 381 CG LEU 52 43.808 45.589 51.097 1.00 19.14 DIC ATOM 382 CD1 LEU 52 43.488 44.439 52.019 1.00 19.58 DIC ATOM 383 CD2 LEU 52 43.344 46.896 51.694 1.00 19.21 DIC ATOM 384 C LEU 52 47.195 46.798 49.645 1.00 23.35 DIC ATOM 385 O LEU 52 47.703 46.358 48.611 1.00 23.99 DIC ATOM 386 N ARG 53 47.896 47.337 50.639 1.00 25.01 DIC ATOM 387 CA ARG 53 49.346 47.509 50.589 1.00 27.42 DIC ATOM 388 CB ARG 53 49.894 47.695 52.012 1.00 26.42 DIC ATOM 389 CG ARG 53 50.983 48.739 52.099 1.00 25.31 DIC ATOM 390 CD ARG 53 50.808 49.649 53.310 1.00 24.31 DIC ATOM 391 NE ARG 53 50.903 48.918 54.567 1.00 22.35 DIC ATOM 392 CZ ARG 53 50.893 49.492 55.766 1.00 21.59 DIC ATOM 393 NH1 ARG 53 50.791 50.811 55.878 1.00 20.50 DIC ATOM 394 NH2 ARG 53 50.987 48.741 56.854 1.00 20.22 DIC ATOM 395 C ARG 53 50.089 46.390 49.875 1.00 28.67 DIC ATOM 396 O ARG 53 50.483 46.536 48.717 1.00 29.49 DIC ATOM 397 N GLY 55 50.292 45.278 50.563 1.00 30.50 DIC ATOM 398 CA GLY 55 50.987 44.173 49.937 1.00 32.29 DIC ATOM 399 C GLY 55 49.974 43.171 49.431 1.00 33.53 DIC ATOM 400 O GLY 55 50.312 42.264 48.663 1.00 34.18 DIC ATOM 401 N GLY 56 48.724 43.351 49.857 1.00 33.60 DIC ATOM 402 CA GLY 56 47.659 42.445 49.462 1.00 33.15 DIC ATOM 403 C GLY 56 47.872 41.107 50.146 1.00 33.10 DIC ATOM 404 O GLY 56 46.962 40.273 50.215 1.00 33.20 DIC ATOM 405 N GLY 57 49.088 40.914 50.656 1.00 32.04 DIC ATOM 406 CA GLY 57 49.447 39.682 51.333 1.00 30.83 DIC ATOM 407 C GLY 57 49.086 39.682 52.804 1.00 29.47 DIC ATOM 408 O GLY 57 49.138 38.640 53.457 1.00 30.37 DIC ATOM 409 N ASN 58 48.726 40.843 53.341 1.00 28.08 DIC ATOM 410 CA ASN 58 48.353 40.905 54.747 1.00 26.03 DIC ATOM 411 CB ASN 58 48.987 42.120 55.427 1.00 27.85 DIC ATOM 412 CG ASN 58 50.322 41.789 56.080 1.00 29.56 DIC ATOM 413 OD1 ASN 58 50.447 40.787 56.791 1.00 30.26 DIC ATOM 414 ND2 ASN 58 51.325 42.635 55.852 1.00 30.45 DIC ATOM 415 C ASN 58 46.845 40.893 54.995 1.00 24.13 DIC ATOM 416 O ASN 58 46.347 41.597 55.872 1.00 23.13 DIC ATOM 417 N ILE 59 46.114 40.099 54.217 1.00 20.72 DIC ATOM 418 CA ILE 59 44.678 39.992 54.423 1.00 19.23 DIC ATOM 419 CB ILE 59 43.873 40.915 53.471 1.00 19.07 DIC ATOM 420 CG2 ILE 59 44.100 40.511 52.016 1.00 18.83 DIC ATOM 421 CG1 ILE 59 42.387 40.848 53.838 1.00 18.98 DIC ATOM 422 CD ILE 59 41.510 41.865 53.110 1.00 19.26 DIC ATOM 423 C ILE 59 44.213 38.551 54.259 1.00 18.23 DIC ATOM 424 O ILE 59 44.446 37.916 53.233 1.00 17.66 DIC ATOM 425 N ARG 60 43.561 38.035 55.289 1.00 17.86 DIC ATOM 426 CA ARG 60 43.065 36.667 55.267 1.00 17.16 DIC ATOM 427 CB ARG 60 43.768 35.845 56.355 1.00 18.42 DIC ATOM 428 CG ARG 60 43.308 34.401 56.461 1.00 21.63 DIC ATOM 429 CD ARG 60 44.434 33.455 56.908 1.00 25.56 DIC ATOM 430 NE ARG 60 44.956 33.771 58.234 1.00 29.10 DIC ATOM 431 CZ ARG 60 45.878 34.698 58.483 1.00 31.08 DIC ATOM 432 NH1 ARG 60 46.397 35.411 57.489 1.00 32.55 DIC ATOM 433 NH2 ARG 60 46.277 34.922 59.730 1.00 31.29 DIC ATOM 434 C ARG 60 41.564 36.668 55.491 1.00 16.93 DIC ATOM 435 O ARG 60 41.067 37.309 56.422 1.00 16.37 DIC ATOM 436 N PHE 61 40.834 35.967 54.629 1.00 14.83 DIC ATOM 437 CA PHE 61 39.391 35.895 54.777 1.00 15.90 DIC ATOM 438 CB PHE 61 38.705 35.931 53.413 1.00 14.84 DIC ATOM 439 CG PHE 61 38.919 37.215 52.670 1.00 13.10 DIC ATOM 440 CD1 PHE 61 40.034 37.389 51.862 1.00 14.08 DIC ATOM 441 CD2 PHE 61 38.010 38.258 52.793 1.00 12.89 DIC ATOM 442 CE1 PHE 61 40.241 38.585 51.185 1.00 13.50 DIC ATOM 443 CE2 PHE 61 38.206 39.457 52.121 1.00 12.60 DIC ATOM 444 CZ PHE 61 39.322 39.623 51.316 1.00 13.60 DIC ATOM 445 C PHE 61 39.022 34.624 55.520 1.00 15.95 DIC ATOM 446 O PHE 61 39.541 33.555 55.221 1.00 15.87 DIC ATOM 447 N ILE 62 38.131 34.750 56.498 1.00 16.48 DIC ATOM 448 CA ILE 62 37.709 33.611 57.304 1.00 16.08 DIC ATOM 449 CB ILE 62 37.979 33.864 58.801 1.00 15.26 DIC ATOM 450 CG2 ILE 62 37.698 32.604 59.611 1.00 13.49 DIC ATOM 451 CG1 ILE 62 39.428 34.292 59.002 1.00 14.70 DIC ATOM 452 CD ILE 62 39.692 34.939 60.347 1.00 14.47 DIC ATOM 453 C ILE 62 36.220 33.360 57.123 1.00 17.10 DIC ATOM 454 O ILE 62 35.385 34.154 57.558 1.00 16.19 DIC ATOM 455 N ASP 63 35.895 32.242 56.489 1.00 18.05 DIC ATOM 456 CA ASP 63 34.511 31.883 56.245 1.00 18.87 DIC ATOM 457 CB ASP 63 34.451 30.589 55.420 1.00 21.18 DIC ATOM 458 CG ASP 63 34.653 30.834 53.932 1.00 22.82 DIC ATOM 459 OD1 ASP 63 35.479 31.697 53.565 1.00 23.93 DIC ATOM 460 OD2 ASP 63 33.986 30.157 53.127 1.00 23.20 DIC ATOM 461 C ASP 63 33.712 31.708 57.530 1.00 18.75 DIC ATOM 462 O ASP 63 34.127 31.004 58.448 1.00 18.31 DIC ATOM 463 N VAL 64 32.570 32.377 57.595 1.00 18.18 DIC ATOM 464 CA VAL 64 31.681 32.258 58.739 1.00 17.99 DIC ATOM 465 CB VAL 64 31.571 33.582 59.544 1.00 17.92 DIC ATOM 466 CG1 VAL 64 32.939 33.989 60.053 1.00 17.77 DIC ATOM 467 CG2 VAL 64 30.960 34.681 58.694 1.00 16.70 DIC ATOM 468 C VAL 64 30.325 31.889 58.161 1.00 17.88 DIC ATOM 469 O VAL 64 29.990 32.298 57.049 1.00 18.31 DIC ATOM 470 N ASN 65 29.562 31.085 58.891 1.00 17.42 DIC ATOM 471 CA ASN 65 28.241 30.685 58.430 1.00 17.62 DIC ATOM 472 CB ASN 65 27.924 29.261 58.885 1.00 18.50 DIC ATOM 473 CG ASN 65 26.616 28.743 58.306 1.00 20.54 DIC ATOM 474 OD1 ASN 65 25.714 29.521 57.968 1.00 20.86 DIC ATOM 475 ND2 ASN 65 26.499 27.420 58.200 1.00 19.60 DIC ATOM 476 C ASN 65 27.227 31.652 59.035 1.00 17.64 DIC ATOM 477 O ASN 65 26.932 31.585 60.230 1.00 16.65 DIC ATOM 478 N PRO 66 26.675 32.565 58.219 1.00 17.39 DIC ATOM 479 CD PRO 66 26.861 32.781 56.774 1.00 17.24 DIC ATOM 480 CA PRO 66 25.703 33.510 58.769 1.00 18.54 DIC ATOM 481 CB PRO 66 25.296 34.347 57.551 1.00 18.56 DIC ATOM 482 CG PRO 66 25.566 33.444 56.388 1.00 17.52 DIC ATOM 483 C PRO 66 24.516 32.866 59.480 1.00 19.19 DIC ATOM 484 O PRO 66 24.040 33.396 60.479 1.00 19.74 DIC ATOM 485 N ALA 67 24.058 31.717 58.984 1.00 19.24 DIC ATOM 486 CA ALA 67 22.913 31.029 59.583 1.00 18.98 DIC ATOM 487 CB ALA 67 22.603 29.740 58.805 1.00 19.76 DIC ATOM 488 C ALA 67 23.117 30.710 61.062 1.00 18.67 DIC ATOM 489 O ALA 67 22.154 30.496 61.797 1.00 18.27 DIC ATOM 490 N ASP 68 24.370 30.678 61.497 1.00 18.15 DIC ATOM 491 CA ASP 68 24.672 30.382 62.892 1.00 17.77 DIC ATOM 492 CB ASP 68 26.176 30.488 63.148 1.00 18.64 DIC ATOM 493 CG ASP 68 26.963 29.362 62.507 1.00 19.18 DIC ATOM 494 OD1 ASP 68 28.206 29.374 62.630 1.00 19.68 DIC ATOM 495 OD2 ASP 68 26.349 28.466 61.889 1.00 19.92 DIC ATOM 496 C ASP 68 23.948 31.307 63.868 1.00 17.23 DIC ATOM 497 O ASP 68 23.621 30.908 64.986 1.00 14.77 DIC ATOM 498 N PHE 69 23.705 32.544 63.452 1.00 17.46 DIC ATOM 499 CA PHE 69 23.061 33.513 64.332 1.00 18.56 DIC ATOM 500 CB PHE 69 23.895 34.801 64.374 1.00 19.00 DIC ATOM 501 CG PHE 69 25.382 34.558 64.338 1.00 18.44 DIC ATOM 502 CD1 PHE 69 26.069 34.550 63.126 1.00 18.34 DIC ATOM 503 CD2 PHE 69 26.080 34.274 65.506 1.00 17.81 DIC ATOM 504 CE1 PHE 69 27.435 34.256 63.081 1.00 17.68 DIC ATOM 505 CE2 PHE 69 27.441 33.980 65.477 1.00 17.08 DIC ATOM 506 CZ PHE 69 28.122 33.968 64.264 1.00 17.08 DIC ATOM 507 C PHE 69 21.642 33.825 63.889 1.00 19.64 DIC ATOM 508 O PHE 69 21.075 34.854 64.259 1.00 18.70 DIC ATOM 509 N ALA 70 21.067 32.919 63.109 1.00 20.08 DIC ATOM 510 CA ALA 70 19.718 33.094 62.593 1.00 21.26 DIC ATOM 511 CB ALA 70 19.302 31.846 61.818 1.00 22.16 DIC ATOM 512 C ALA 70 18.664 33.419 63.654 1.00 21.75 DIC ATOM 513 O ALA 70 17.783 34.246 63.421 1.00 22.84 DIC ATOM 514 N GLY 71 18.753 32.775 64.813 1.00 20.77 DIC ATOM 515 CA GLY 71 17.773 33.010 65.861 1.00 20.62 DIC ATOM 516 C GLY 71 17.817 34.344 66.599 1.00 20.26 DIC ATOM 517 O GLY 71 16.882 34.670 67.342 1.00 19.68 DIC ATOM 518 N PHE 72 18.878 35.120 66.392 1.00 18.49 DIC ATOM 519 CA PHE 72 19.042 36.412 67.063 1.00 17.73 DIC ATOM 520 CB PHE 72 20.536 36.763 67.145 1.00 18.72 DIC ATOM 521 CG PHE 72 21.348 35.802 67.980 1.00 20.16 DIC ATOM 522 CD1 PHE 72 22.724 35.960 68.097 1.00 20.37 DIC ATOM 523 CD2 PHE 72 20.737 34.760 68.668 1.00 20.44 DIC ATOM 524 CE1 PHE 72 23.477 35.100 68.888 1.00 21.46 DIC ATOM 525 CE2 PHE 72 21.484 33.892 69.462 1.00 21.52 DIC ATOM 526 CZ PHE 72 22.858 34.065 69.572 1.00 20.60 DIC ATOM 527 C PHE 72 18.274 37.551 66.386 1.00 16.90 DIC ATOM 528 O PHE 72 18.171 37.603 65.163 1.00 16.76 DIC ATOM 529 N PRO 73 17.738 38.492 67.176 1.00 16.37 DIC ATOM 530 CD PRO 73 17.908 38.675 68.626 1.00 16.89 DIC ATOM 531 CA PRO 73 16.984 39.609 66.600 1.00 16.59 DIC ATOM 532 CB PRO 73 16.616 40.447 67.825 1.00 16.80 DIC ATOM 533 CG PRO 73 17.705 40.164 68.773 1.00 17.34 DIC ATOM 534 C PRO 73 17.720 40.419 65.537 1.00 16.70 DIC ATOM 535 O PRO 73 18.924 40.645 65.629 1.00 15.30 DIC ATOM 536 N LEU 74 16.980 40.839 64.517 1.00 16.98 DIC ATOM 537 CA LEU 74 17.548 41.634 63.434 1.00 17.87 DIC ATOM 538 CB LEU 74 17.843 40.730 62.234 1.00 17.95 DIC ATOM 539 CG LEU 74 18.954 41.199 61.293 1.00 17.88 DIC ATOM 540 CD1 LEU 74 20.295 41.203 62.038 1.00 18.31 DIC ATOM 541 CD2 LEU 74 19.023 40.272 60.092 1.00 19.47 DIC ATOM 542 C LEU 74 16.520 42.713 63.068 1.00 18.09 DIC ATOM 543 O LEU 74 15.955 42.709 61.972 1.00 19.62 DIC ATOM 544 N ASN 75 16.290 43.630 64.005 1.00 17.72 DIC ATOM 545 CA ASN 75 15.322 44.715 63.846 1.00 17.11 DIC ATOM 546 CB ASN 75 14.735 45.110 65.229 1.00 17.62 DIC ATOM 547 CG ASN 75 15.817 45.329 66.338 1.00 20.20 DIC ATOM 548 OD1 ASN 75 16.525 44.396 66.744 1.00 19.66 DIC ATOM 549 ND2 ASN 75 15.911 46.566 66.844 1.00 20.31 DIC ATOM 550 C ASN 75 15.830 45.971 63.124 1.00 16.07 DIC ATOM 551 O ASN 75 15.053 46.683 62.477 1.00 15.53 DIC ATOM 552 N ILE 76 17.123 46.244 63.238 1.00 13.71 DIC ATOM 553 CA ILE 76 17.706 47.421 62.606 1.00 11.78 DIC ATOM 554 CB ILE 76 19.043 47.771 63.295 1.00 10.80 DIC ATOM 555 CG2 ILE 76 19.621 49.050 62.717 1.00 10.89 DIC ATOM 556 CG1 ILE 76 18.784 47.965 64.795 1.00 11.97 DIC ATOM 557 CD ILE 76 20.028 48.230 65.615 1.00 11.60 DIC ATOM 558 C ILE 76 17.880 47.165 61.112 1.00 10.59 DIC ATOM 559 O ILE 76 18.735 46.393 60.692 1.00 9.86 DIC ATOM 560 N ARG 77 17.047 47.823 60.312 1.00 10.58 DIC ATOM 561 CA ARG 77 17.046 47.629 58.865 1.00 9.71 DIC ATOM 562 CB ARG 77 16.017 48.560 58.224 1.00 10.51 DIC ATOM 563 CG ARG 77 15.694 48.227 56.770 1.00 12.15 DIC ATOM 564 CD ARG 77 14.702 49.229 56.194 1.00 14.05 DIC ATOM 565 NE ARG 77 14.405 48.956 54.792 1.00 15.41 DIC ATOM 566 CZ ARG 77 14.025 49.879 53.915 1.00 15.57 DIC ATOM 567 NH1 ARG 77 13.894 51.145 54.291 1.00 16.47 DIC ATOM 568 NH2 ARG 77 13.783 49.537 52.660 1.00 16.39 DIC ATOM 569 C ARG 77 18.370 47.769 58.125 1.00 9.25 DIC ATOM 570 O ARG 77 18.662 46.979 57.228 1.00 8.24 DIC ATOM 571 N HIS 78 19.175 48.765 58.475 1.00 9.54 DIC ATOM 572 CA HIS 78 20.435 48.953 57.763 1.00 9.73 DIC ATOM 573 CB HIS 78 20.945 50.392 57.948 1.00 9.99 DIC ATOM 574 CG HIS 78 21.495 50.677 59.313 1.00 9.83 DIC ATOM 575 CD2 HIS 78 20.910 51.193 60.417 1.00 9.26 DIC ATOM 576 ND1 HIS 78 22.801 50.399 59.664 1.00 12.11 DIC ATOM 577 CE1 HIS 78 22.992 50.731 60.927 1.00 10.27 DIC ATOM 578 NE2 HIS 78 21.860 51.213 61.407 1.00 10.71 DIC ATOM 579 C HIS 78 21.518 47.956 58.160 1.00 9.77 DIC ATOM 580 O HIS 78 22.634 48.014 57.643 1.00 9.16 DIC ATOM 581 N ILE 79 21.186 47.018 59.046 1.00 8.59 DIC ATOM 582 CA ILE 79 22.176 46.041 59.499 1.00 9.47 DIC ATOM 583 CB ILE 79 22.352 46.115 61.036 1.00 8.92 DIC ATOM 584 CG2 ILE 79 23.362 45.071 61.497 1.00 9.10 DIC ATOM 585 CG1 ILE 79 22.817 47.519 61.444 1.00 8.56 DIC ATOM 586 CD ILE 79 22.873 47.729 62.947 1.00 7.54 DIC ATOM 587 C ILE 79 21.855 44.597 59.129 1.00 9.95 DIC ATOM 588 O ILE 79 20.745 44.118 59.370 1.00 9.89 DIC ATOM 589 N SER 80 22.834 43.897 58.558 1.00 10.77 DIC ATOM 590 CA SER 80 22.644 42.489 58.185 1.00 10.59 DIC ATOM 591 CB SER 80 23.405 42.148 56.896 1.00 11.09 DIC ATOM 592 OG SER 80 24.799 42.152 57.115 1.00 11.31 DIC ATOM 593 C SER 80 23.102 41.551 59.304 1.00 10.27 DIC ATOM 594 O SER 80 23.784 41.967 60.250 1.00 9.68 DIC ATOM 595 N ILE 81 22.719 40.282 59.181 1.00 9.94 DIC ATOM 596 CA ILE 81 23.035 39.260 60.167 1.00 10.92 DIC ATOM 597 CB ILE 81 22.450 37.880 59.731 1.00 10.93 DIC ATOM 598 CG2 ILE 81 23.161 37.384 58.480 1.00 10.14 DIC ATOM 599 CG1 ILE 81 22.602 36.851 60.856 1.00 11.94 DIC ATOM 600 CD ILE 81 21.957 37.263 62.171 1.00 14.84 DIC ATOM 601 C ILE 81 24.530 39.131 60.452 1.00 10.21 DIC ATOM 602 O ILE 81 24.914 38.697 61.527 1.00 10.54 DIC ATOM 603 N THR 82 25.370 39.530 59.504 1.00 10.02 DIC ATOM 604 CA THR 82 26.814 39.440 59.690 1.00 11.39 DIC ATOM 605 CB THR 82 27.562 39.940 58.441 1.00 11.65 DIC ATOM 606 OG1 THR 82 27.204 39.125 57.325 1.00 14.61 DIC ATOM 607 CG2 THR 82 29.065 39.859 58.646 1.00 12.44 DIC ATOM 608 C THR 82 27.294 40.228 60.909 1.00 10.13 DIC ATOM 609 O THR 82 28.376 39.972 61.438 1.00 11.18 DIC ATOM 610 N THR 83 26.490 41.184 61.352 1.00 9.24 DIC ATOM 611 CA THR 83 26.839 41.991 62.518 1.00 8.73 DIC ATOM 612 CB THR 83 25.721 43.017 62.837 1.00 8.11 DIC ATOM 613 OG1 THR 83 26.189 43.930 63.833 1.00 6.94 DIC ATOM 614 CG2 THR 83 24.463 42.316 63.354 1.00 5.65 DIC ATOM 615 C THR 83 27.095 41.143 63.774 1.00 8.48 DIC ATOM 616 O THR 83 27.764 41.597 64.714 1.00 7.40 DIC ATOM 617 N TYR 84 26.571 39.917 63.796 1.00 7.85 DIC ATOM 618 CA TYR 84 26.750 39.036 64.961 1.00 7.48 DIC ATOM 619 CB TYR 84 25.541 38.118 65.149 1.00 8.12 DIC ATOM 620 CG TYR 84 24.309 38.765 65.730 1.00 8.79 DIC ATOM 621 CD1 TYR 84 23.223 39.089 64.920 1.00 8.55 DIC ATOM 622 CE1 TYR 84 22.061 39.639 65.456 1.00 8.25 DIC ATOM 623 CD2 TYR 84 24.208 39.014 67.100 1.00 9.35 DIC ATOM 624 CE2 TYR 84 23.047 39.569 67.647 1.00 8.56 DIC ATOM 625 CZ TYR 84 21.977 39.873 66.813 1.00 8.60 DIC ATOM 626 OH TYR 84 20.811 40.386 67.340 1.00 10.62 DIC ATOM 627 C TYR 84 27.988 38.142 64.917 1.00 7.79 DIC ATOM 628 O TYR 84 28.356 37.544 65.934 1.00 7.52 DIC ATOM 629 N ALA 85 28.631 38.046 63.756 1.00 7.28 DIC ATOM 630 CA ALA 85 29.802 37.172 63.608 1.00 8.87 DIC ATOM 631 CB ALA 85 30.381 37.297 62.200 1.00 8.53 DIC ATOM 632 C ALA 85 30.905 37.410 64.627 1.00 9.13 DIC ATOM 633 O ALA 85 31.639 36.483 64.993 1.00 8.63 DIC ATOM 634 N ARG 86 31.024 38.649 65.082 1.00 9.00 DIC ATOM 635 CA ARG 86 32.065 38.996 66.026 1.00 9.80 DIC ATOM 636 CB ARG 86 32.022 40.502 66.310 1.00 9.41 DIC ATOM 637 CG ARG 86 30.870 40.984 67.172 1.00 9.46 DIC ATOM 638 CD ARG 86 30.719 42.501 67.076 1.00 8.59 DIC ATOM 639 NE ARG 86 29.920 42.881 65.919 1.00 7.42 DIC ATOM 640 CZ ARG 86 29.754 44.128 65.491 1.00 8.59 DIC ATOM 641 NH1 ARG 86 30.342 45.144 66.115 1.00 7.18 DIC ATOM 642 NH2 ARG 86 28.974 44.361 64.449 1.00 9.43 DIC ATOM 643 C ARG 86 31.979 38.185 67.313 1.00 9.79 DIC ATOM 644 O ARG 86 32.978 38.004 68.000 1.00 10.73 DIC ATOM 645 N LEU 87 30.788 37.680 67.624 1.00 10.39 DIC ATOM 646 CA LEU 87 30.584 36.880 68.836 1.00 10.81 DIC ATOM 647 CB LEU 87 29.092 36.574 69.016 1.00 10.20 DIC ATOM 648 CG LEU 87 28.168 37.787 69.233 1.00 10.48 DIC ATOM 649 CD1 LEU 87 26.731 37.315 69.344 1.00 9.48 DIC ATOM 650 CD2 LEU 87 28.579 38.549 70.491 1.00 9.82 DIC ATOM 651 C LEU 87 31.394 35.574 68.884 1.00 10.74 DIC ATOM 652 O LEU 87 31.635 35.036 69.957 1.00 9.80 DIC ATOM 653 N LYS 88 31.811 35.067 67.725 1.00 11.78 DIC ATOM 654 CA LYS 88 32.599 33.831 67.665 1.00 11.01 DIC ATOM 655 CB LYS 88 32.009 32.882 66.612 1.00 11.35 DIC ATOM 656 CG LYS 88 30.771 32.128 67.071 1.00 9.90 DIC ATOM 657 CD LYS 88 30.341 31.114 66.016 1.00 11.02 DIC ATOM 658 CE LYS 88 29.384 30.086 66.593 1.00 10.58 DIC ATOM 659 NZ LYS 88 29.046 29.040 65.576 1.00 11.61 DIC ATOM 660 C LYS 88 34.071 34.097 67.332 1.00 11.82 DIC ATOM 661 O LYS 88 34.782 33.215 66.852 1.00 12.29 DIC ATOM 662 N LEU 89 34.531 35.307 67.611 1.00 12.36 DIC ATOM 663 CA LEU 89 35.902 35.686 67.303 1.00 13.57 DIC ATOM 664 CB LEU 89 36.144 37.121 67.772 1.00 15.15 DIC ATOM 665 CG LEU 89 36.980 38.051 66.888 1.00 16.39 DIC ATOM 666 CD1 LEU 89 36.680 37.846 65.418 1.00 16.80 DIC ATOM 667 CD2 LEU 89 36.684 39.481 67.294 1.00 17.50 DIC ATOM 668 C LEU 89 36.919 34.725 67.918 1.00 13.79 DIC ATOM 669 O LEU 89 37.951 34.420 67.310 1.00 12.41 DIC ATOM 670 N GLY 90 36.615 34.241 69.116 1.00 12.82 DIC ATOM 671 CA GLY 90 37.496 33.303 69.785 1.00 13.31 DIC ATOM 672 C GLY 90 37.608 31.968 69.057 1.00 13.77 DIC ATOM 673 O GLY 90 38.568 31.225 69.270 1.00 12.09 DIC ATOM 674 N GLU 91 36.625 31.662 68.210 1.00 13.93 DIC ATOM 675 CA GLU 91 36.608 30.423 67.431 1.00 14.80 DIC ATOM 676 CB GLU 91 35.172 29.930 67.221 1.00 15.97 DIC ATOM 677 CG GLU 91 34.422 29.493 68.475 1.00 18.54 DIC ATOM 678 CD GLU 91 33.035 28.944 68.145 1.00 20.57 DIC ATOM 679 OE1 GLU 91 32.929 28.123 67.211 1.00 21.70 DIC ATOM 680 OE2 GLU 91 32.057 29.326 68.816 1.00 20.80 DIC ATOM 681 C GLU 91 37.232 30.632 66.050 1.00 14.18 DIC ATOM 682 O GLU 91 37.833 29.717 65.478 1.00 13.91 DIC ATOM 683 N TYR 92 37.076 31.838 65.518 1.00 14.10 DIC ATOM 684 CA TYR 92 37.591 32.171 64.193 1.00 14.43 DIC ATOM 685 CB TYR 92 36.791 33.330 63.595 1.00 13.92 DIC ATOM 686 CG TYR 92 35.306 33.081 63.464 1.00 14.30 DIC ATOM 687 CD1 TYR 92 34.816 31.844 63.032 1.00 14.28 DIC ATOM 688 CE1 TYR 92 33.448 31.630 62.854 1.00 14.75 DIC ATOM 689 CD2 TYR 92 34.392 34.099 63.717 1.00 13.77 DIC ATOM 690 CE2 TYR 92 33.027 33.900 63.539 1.00 15.62 DIC ATOM 691 CZ TYR 92 32.560 32.663 63.105 1.00 14.94 DIC ATOM 692 OH TYR 92 31.213 32.477 62.906 1.00 15.54 DIC ATOM 693 C TYR 92 39.073 32.531 64.108 1.00 14.98 DIC ATOM 694 O TYR 92 39.701 32.328 63.072 1.00 14.45 DIC ATOM 695 N ILE 93 39.629 33.078 65.181 1.00 16.91 DIC ATOM 696 CA ILE 93 41.028 33.486 65.177 1.00 17.72 DIC ATOM 697 CB ILE 93 41.133 35.016 65.393 1.00 18.50 DIC ATOM 698 CG2 ILE 93 42.591 35.432 65.555 1.00 17.36 DIC ATOM 699 CG1 ILE 93 40.487 35.734 64.201 1.00 18.54 DIC ATOM 700 CD ILE 93 40.412 37.226 64.340 1.00 19.24 DIC ATOM 701 C ILE 93 41.858 32.751 66.220 1.00 18.60 DIC ATOM 702 O ILE 93 41.575 32.824 67.419 1.00 19.10 DIC ATOM 703 N ALA 94 42.885 32.043 65.758 1.00 18.48 DIC ATOM 704 CA ALA 94 43.748 31.279 66.651 1.00 20.07 DIC ATOM 705 CB ALA 94 43.905 29.870 66.122 1.00 19.66 DIC ATOM 706 C ALA 94 45.123 31.896 66.856 1.00 20.84 DIC ATOM 707 O ALA 94 45.715 31.768 67.931 1.00 20.49 DIC ATOM 708 N ASP 95 45.625 32.568 65.825 1.00 22.76 DIC ATOM 709 CA ASP 95 46.953 33.177 65.862 1.00 25.64 DIC ATOM 710 CB ASP 95 47.476 33.365 64.430 1.00 27.52 DIC ATOM 711 CG ASP 95 46.420 33.918 63.484 1.00 29.58 DIC ATOM 712 OD1 ASP 95 46.777 34.365 62.374 1.00 31.56 DIC ATOM 713 OD2 ASP 95 45.226 33.898 63.838 1.00 31.61 DIC ATOM 714 C ASP 95 47.129 34.494 66.625 1.00 25.59 DIC ATOM 715 O ASP 95 48.215 35.072 66.591 1.00 27.43 DIC ATOM 716 N CYS 96 46.102 34.967 67.325 1.00 24.71 DIC ATOM 717 CA CYS 96 46.232 36.235 68.043 1.00 23.67 DIC ATOM 718 CB CYS 96 45.513 37.347 67.274 1.00 23.87 DIC ATOM 719 SG CYS 96 46.038 37.496 65.578 1.00 26.37 DIC ATOM 720 C CYS 96 45.728 36.252 69.478 1.00 22.46 DIC ATOM 721 O CYS 96 44.646 35.741 69.776 1.00 22.34 DIC ATOM 722 N ASP 97 46.515 36.858 70.364 1.00 20.39 DIC ATOM 723 CA ASP 97 46.124 36.987 71.762 1.00 20.32 DIC ATOM 724 CB ASP 97 47.354 37.031 72.667 1.00 20.67 DIC ATOM 725 CG ASP 97 47.976 35.667 72.871 1.00 21.98 DIC ATOM 726 OD1 ASP 97 49.035 35.593 73.525 1.00 23.35 DIC ATOM 727 OD2 ASP 97 47.405 34.666 72.386 1.00 23.09 DIC ATOM 728 C ASP 97 45.323 38.279 71.925 1.00 18.84 DIC ATOM 729 O ASP 97 44.574 38.438 72.887 1.00 19.35 DIC ATOM 730 N LYS 98 45.503 39.198 70.978 1.00 16.98 DIC ATOM 731 CA LYS 98 44.814 40.488 70.975 1.00 15.16 DIC ATOM 732 CB LYS 98 45.704 41.580 71.585 1.00 15.88 DIC ATOM 733 CG LYS 98 45.142 42.998 71.424 1.00 16.96 DIC ATOM 734 CD LYS 98 46.102 44.099 71.908 1.00 16.73 DIC ATOM 735 CE LYS 98 46.335 44.046 73.413 1.00 16.78 DIC ATOM 736 NZ LYS 98 47.070 45.241 73.933 1.00 13.95 DIC ATOM 737 C LYS 98 44.479 40.890 69.540 1.00 14.03 DIC ATOM 738 O LYS 98 45.287 40.695 68.637 1.00 13.30 DIC ATOM 739 N VAL 99 43.281 41.431 69.332 1.00 11.95 DIC ATOM 740 CA VAL 99 42.868 41.900 68.012 1.00 11.37 DIC ATOM 741 CB VAL 99 42.024 40.852 67.236 1.00 11.54 DIC ATOM 742 CG1 VAL 99 42.877 39.639 66.882 1.00 11.02 DIC ATOM 743 CG2 VAL 99 40.794 40.453 68.058 1.00 10.46 DIC ATOM 744 C VAL 99 42.021 43.156 68.171 1.00 11.18 DIC ATOM 745 O VAL 99 41.327 43.322 69.171 1.00 10.93 DIC ATOM 746 N LEU 100 42.095 44.044 67.187 1.00 10.87 DIC ATOM 747 CA LEU 100 41.314 45.271 67.212 1.00 10.79 DIC ATOM 748 CB LEU 100 42.197 46.484 66.880 1.00 10.94 DIC ATOM 749 CG LEU 100 41.529 47.869 66.831 1.00 12.58 DIC ATOM 750 CD1 LEU 100 40.633 48.068 68.043 1.00 11.52 DIC ATOM 751 CD2 LEU 100 42.601 48.949 66.788 1.00 13.16 DIC ATOM 752 C LEU 100 40.219 45.108 66.169 1.00 10.87 DIC ATOM 753 O LEU 100 40.499 45.034 64.964 1.00 10.41 DIC ATOM 754 N TYR 101 38.981 45.026 66.651 1.00 10.75 DIC ATOM 755 CA TYR 101 37.811 44.861 65.806 1.00 10.15 DIC ATOM 756 CB TYR 101 36.714 44.096 66.553 1.00 11.92 DIC ATOM 757 CG TYR 101 35.519 43.787 65.679 1.00 12.22 DIC ATOM 758 CD1 TYR 101 35.489 42.629 64.912 1.00 13.77 DIC ATOM 759 CE1 TYR 101 34.442 42.355 64.055 1.00 14.00 DIC ATOM 760 CD2 TYR 101 34.452 44.677 65.566 1.00 13.42 DIC ATOM 761 CE2 TYR 101 33.377 44.409 64.690 1.00 13.71 DIC ATOM 762 CZ TYR 101 33.390 43.240 63.944 1.00 14.55 DIC ATOM 763 OH TYR 101 32.356 42.920 63.085 1.00 16.39 DIC ATOM 764 C TYR 101 37.251 46.216 65.411 1.00 10.17 DIC ATOM 765 O TYR 101 37.062 47.088 66.267 1.00 8.43 DIC ATOM 766 N LEU 102 36.972 46.385 64.121 1.00 8.96 DIC ATOM 767 CA LEU 102 36.409 47.629 63.617 1.00 9.15 DIC ATOM 768 CB LEU 102 37.429 48.370 62.757 1.00 9.36 DIC ATOM 769 CG LEU 102 38.760 48.796 63.379 1.00 10.19 DIC ATOM 770 CD1 LEU 102 39.640 49.399 62.292 1.00 9.39 DIC ATOM 771 CD2 LEU 102 38.507 49.791 64.514 1.00 9.64 DIC ATOM 772 C LEU 102 35.182 47.341 62.757 1.00 9.25 DIC ATOM 773 O LEU 102 35.178 46.379 61.988 1.00 9.46 DIC ATOM 774 N ASP 103 34.141 48.160 62.902 1.00 7.67 DIC ATOM 775 CA ASP 103 32.942 48.022 62.074 1.00 6.79 DIC ATOM 776 CB ASP 103 31.854 49.000 62.505 1.00 6.14 DIC ATOM 777 CG ASP 103 30.853 48.392 63.452 1.00 6.30 DIC ATOM 778 OD1 ASP 103 29.900 49.112 63.821 1.00 6.96 DIC ATOM 779 OD2 ASP 103 31.013 47.212 63.831 1.00 6.76 DIC ATOM 780 C ASP 103 33.407 48.438 60.689 1.00 6.85 DIC ATOM 781 O ASP 103 34.500 48.972 60.536 1.00 6.31 DIC ATOM 782 N ILE 104 32.564 48.234 59.690 1.00 8.06 DIC ATOM 783 CA ILE 104 32.914 48.593 58.318 1.00 7.88 DIC ATOM 784 CB ILE 104 32.057 47.796 57.315 1.00 9.07 DIC ATOM 785 CG2 ILE 104 32.357 48.246 55.891 1.00 9.25 DIC ATOM 786 CG1 ILE 104 32.297 46.290 57.504 1.00 8.98 DIC ATOM 787 CD ILE 104 33.728 45.819 57.279 1.00 9.78 DIC ATOM 788 C ILE 104 32.697 50.077 58.058 1.00 8.07 DIC ATOM 789 O ILE 104 33.375 50.675 57.223 1.00 7.27 DIC ATOM 790 N ASP 105 31.747 50.663 58.778 1.00 7.66 DIC ATOM 791 CA ASP 105 31.412 52.075 58.630 1.00 8.00 DIC ATOM 792 CB ASP 105 29.941 52.304 59.001 1.00 6.68 DIC ATOM 793 CG ASP 105 29.618 51.884 60.426 1.00 5.32 DIC ATOM 794 OD1 ASP 105 30.399 51.116 61.034 1.00 5.29 DIC ATOM 795 OD2 ASP 105 28.555 52.303 60.942 1.00 5.88 DIC ATOM 796 C ASP 105 32.303 52.991 59.469 1.00 8.38 DIC ATOM 797 O ASP 105 31.811 53.904 60.140 1.00 8.29 DIC ATOM 798 N VAL 106 33.609 52.733 59.437 1.00 9.42 DIC ATOM 799 CA VAL 106 34.565 53.552 60.170 1.00 10.80 DIC ATOM 800 CB VAL 106 35.344 52.758 61.252 1.00 11.19 DIC ATOM 801 CG1 VAL 106 34.380 52.108 62.219 1.00 10.51 DIC ATOM 802 CG2 VAL 106 36.258 51.732 60.595 1.00 11.56 DIC ATOM 803 C VAL 106 35.585 54.115 59.201 1.00 11.38 DIC ATOM 804 O VAL 106 35.790 53.579 58.112 1.00 10.35 DIC ATOM 805 N LEU 107 36.227 55.194 59.623 1.00 12.57 DIC ATOM 806 CA LEU 107 37.249 55.860 58.833 1.00 13.47 DIC ATOM 807 CB LEU 107 36.648 57.092 58.159 1.00 13.56 DIC ATOM 808 CG LEU 107 36.761 57.246 56.639 1.00 15.06 DIC ATOM 809 CD1 LEU 107 36.504 55.925 55.932 1.00 14.78 DIC ATOM 810 CD2 LEU 107 35.761 58.311 56.183 1.00 15.25 DIC ATOM 811 C LEU 107 38.346 56.262 59.820 1.00 13.50 DIC ATOM 812 O LEU 107 38.173 57.193 60.602 1.00 13.59 DIC ATOM 813 N VAL 108 39.457 55.532 59.798 1.00 13.84 DIC ATOM 814 CA VAL 108 40.581 55.799 60.689 1.00 14.29 DIC ATOM 815 CB VAL 108 41.566 54.613 60.695 1.00 13.17 DIC ATOM 816 CG1 VAL 108 42.776 54.931 61.572 1.00 11.37 DIC ATOM 817 CG2 VAL 108 40.866 53.378 61.199 1.00 11.78 DIC ATOM 818 C VAL 108 41.303 57.050 60.223 1.00 15.14 DIC ATOM 819 O VAL 108 41.829 57.080 59.111 1.00 15.87 DIC ATOM 820 N ARG 109 41.336 58.077 61.072 1.00 16.17 DIC ATOM 821 CA ARG 109 41.975 59.341 60.711 1.00 16.20 DIC ATOM 822 CB ARG 109 41.024 60.505 60.978 1.00 18.37 DIC ATOM 823 CG ARG 109 39.558 60.117 61.037 1.00 21.36 DIC ATOM 824 CD ARG 109 38.713 61.006 60.157 1.00 23.86 DIC ATOM 825 NE ARG 109 39.024 62.420 60.326 1.00 26.81 DIC ATOM 826 CZ ARG 109 38.490 63.389 59.584 1.00 27.63 DIC ATOM 827 NH1 ARG 109 38.828 64.653 59.792 1.00 28.71 DIC ATOM 828 NH2 ARG 109 37.614 63.089 58.635 1.00 27.97 DIC ATOM 829 C ARG 109 43.284 59.610 61.444 1.00 15.84 DIC ATOM 830 O ARG 109 43.962 60.596 61.159 1.00 15.77 DIC ATOM 831 N ASP 110 43.623 58.758 62.401 1.00 14.29 DIC ATOM 832 CA ASP 110 44.854 58.930 63.156 1.00 14.80 DIC ATOM 833 CB ASP 110 44.643 59.920 64.309 1.00 15.65 DIC ATOM 834 CG ASP 110 45.953 60.434 64.894 1.00 17.51 DIC ATOM 835 OD1 ASP 110 46.918 60.646 64.127 1.00 18.17 DIC ATOM 836 OD2 ASP 110 46.019 60.651 66.121 1.00 17.67 DIC ATOM 837 C ASP 110 45.302 57.577 63.683 1.00 15.01 DIC ATOM 838 O ASP 110 44.514 56.635 63.761 1.00 13.14 DIC ATOM 839 N ARG 111 46.580 57.493 64.026 1.00 15.41 DIC ATOM 840 CA ARG 111 47.185 56.274 64.532 1.00 15.96 DIC ATOM 841 CB ARG 111 48.589 56.587 65.040 1.00 18.93 DIC ATOM 842 CG ARG 111 49.292 55.406 65.638 1.00 21.10 DIC ATOM 843 CD ARG 111 49.885 55.785 66.979 1.00 26.48 DIC ATOM 844 NE ARG 111 50.917 56.811 66.896 1.00 29.16 DIC ATOM 845 CZ ARG 111 51.589 57.267 67.946 1.00 29.73 DIC ATOM 846 NH1 ARG 111 51.332 56.778 69.155 1.00 30.77 DIC ATOM 847 NH2 ARG 111 52.514 58.211 67.789 1.00 30.14 DIC ATOM 848 C ARG 111 46.381 55.601 65.643 1.00 15.25 DIC ATOM 849 O ARG 111 45.870 56.266 66.543 1.00 13.85 DIC ATOM 850 N LEU 112 46.294 54.275 65.572 1.00 13.25 DIC ATOM 851 CA LEU 112 45.569 53.467 66.555 1.00 13.07 DIC ATOM 852 CB LEU 112 44.820 52.336 65.845 1.00 12.62 DIC ATOM 853 CG LEU 112 43.346 52.448 65.422 1.00 13.47 DIC ATOM 854 CD1 LEU 112 42.780 53.836 65.654 1.00 11.94 DIC ATOM 855 CD2 LEU 112 43.243 52.037 63.970 1.00 13.50 DIC ATOM 856 C LEU 112 46.508 52.850 67.593 1.00 12.50 DIC ATOM 857 O LEU 112 46.067 52.151 68.497 1.00 11.71 DIC ATOM 858 N THR 113 47.802 53.107 67.462 1.00 11.56 DIC ATOM 859 CA THR 113 48.783 52.539 68.380 1.00 12.01 DIC ATOM 860 CB THR 113 50.184 53.060 68.041 1.00 11.89 DIC ATOM 861 OG1 THR 113 50.408 52.885 66.634 1.00 11.98 DIC ATOM 862 CG2 THR 113 51.261 52.293 68.820 1.00 13.32 DIC ATOM 863 C THR 113 48.475 52.770 69.864 1.00 12.09 DIC ATOM 864 O THR 113 48.600 51.851 70.672 1.00 13.00 DIC ATOM 865 N PRO 114 48.071 53.997 70.246 1.00 11.73 DIC ATOM 866 CD PRO 114 48.006 55.257 69.488 1.00 11.33 DIC ATOM 867 CA PRO 114 47.764 54.227 71.662 1.00 12.05 DIC ATOM 868 CB PRO 114 47.313 55.685 71.685 1.00 11.93 DIC ATOM 869 CG PRO 114 48.143 56.295 70.585 1.00 12.09 DIC ATOM 870 C PRO 114 46.674 53.271 72.150 1.00 11.56 DIC ATOM 871 O PRO 114 46.743 52.757 73.266 1.00 11.37 DIC ATOM 872 N LEU 115 45.664 53.037 71.314 1.00 10.81 DIC ATOM 873 CA LEU 115 44.590 52.120 71.683 1.00 10.71 DIC ATOM 874 CB LEU 115 43.423 52.211 70.689 1.00 10.70 DIC ATOM 875 CG LEU 115 42.277 51.209 70.886 1.00 10.89 DIC ATOM 876 CD1 LEU 115 41.718 51.306 72.293 1.00 11.32 DIC ATOM 877 CD2 LEU 115 41.184 51.495 69.857 1.00 10.96 DIC ATOM 878 C LEU 115 45.150 50.703 71.693 1.00 9.83 DIC ATOM 879 O LEU 115 44.966 49.967 72.648 1.00 11.08 DIC ATOM 880 N TRP 116 45.850 50.338 70.628 1.00 9.48 DIC ATOM 881 CA TRP 116 46.436 49.007 70.511 1.00 10.20 DIC ATOM 882 CB TRP 116 47.167 48.873 69.164 1.00 9.44 DIC ATOM 883 CG TRP 116 47.899 47.551 68.983 1.00 10.50 DIC ATOM 884 CD2 TRP 116 47.327 46.288 68.606 1.00 10.45 DIC ATOM 885 CE2 TRP 116 48.374 45.337 68.603 1.00 11.26 DIC ATOM 886 CE3 TRP 116 46.033 45.869 68.276 1.00 11.37 DIC ATOM 887 CD1 TRP 116 49.228 47.320 69.185 1.00 10.48 DIC ATOM 888 NE1 TRP 116 49.522 45.992 68.956 1.00 11.48 DIC ATOM 889 CZ2 TRP 116 48.166 43.988 68.276 1.00 10.98 DIC ATOM 890 CZ3 TRP 116 45.827 44.529 67.951 1.00 10.53 DIC ATOM 891 CH2 TRP 116 46.892 43.605 67.954 1.00 9.77 DIC ATOM 892 C TRP 116 47.388 48.674 71.662 1.00 11.01 DIC ATOM 893 O TRP 116 47.439 47.533 72.117 1.00 11.69 DIC ATOM 894 N ASP 117 48.133 49.667 72.138 1.00 11.59 DIC ATOM 895 CA ASP 117 49.084 49.442 73.223 1.00 12.22 DIC ATOM 896 CB ASP 117 50.162 50.534 73.238 1.00 12.26 DIC ATOM 897 CG ASP 117 51.120 50.425 72.077 1.00 13.59 DIC ATOM 898 OD1 ASP 117 51.257 49.321 71.515 1.00 12.25 DIC ATOM 899 OD2 ASP 117 51.752 51.449 71.745 1.00 14.88 DIC ATOM 900 C ASP 117 48.438 49.390 74.599 1.00 13.46 DIC ATOM 901 O ASP 117 49.125 49.168 75.598 1.00 13.16 DIC ATOM 902 N THR 118 47.127 49.606 74.660 1.00 14.71 DIC ATOM 903 CA THR 118 46.425 49.575 75.939 1.00 16.37 DIC ATOM 904 CB THR 118 44.938 49.978 75.779 1.00 16.43 DIC ATOM 905 OG1 THR 118 44.862 51.305 75.244 1.00 16.77 DIC ATOM 906 CG2 THR 118 44.220 49.948 77.129 1.00 17.74 DIC ATOM 907 C THR 118 46.494 48.183 76.555 1.00 17.33 DIC ATOM 908 O THR 118 46.284 47.184 75.871 1.00 16.96 DIC ATOM 909 N ASP 119 46.792 48.123 77.849 1.00 18.74 DIC ATOM 910 CA ASP 119 46.871 46.843 78.552 1.00 20.28 DIC ATOM 911 CB ASP 119 47.930 46.919 79.656 1.00 22.23 DIC ATOM 912 CG ASP 119 47.948 45.685 80.536 1.00 24.82 DIC ATOM 913 OD1 ASP 119 47.718 44.570 80.020 1.00 25.22 DIC ATOM 914 OD2 ASP 119 48.211 45.832 81.750 1.00 27.28 DIC ATOM 915 C ASP 119 45.496 46.519 79.137 1.00 20.16 DIC ATOM 916 O ASP 119 45.038 47.173 80.076 1.00 19.67 DIC ATOM 917 N LEU 120 44.844 45.511 78.565 1.00 19.65 DIC ATOM 918 CA LEU 120 43.505 45.102 78.985 1.00 19.29 DIC ATOM 919 CB LEU 120 42.851 44.242 77.892 1.00 18.66 DIC ATOM 920 CG LEU 120 42.554 44.848 76.517 1.00 18.25 DIC ATOM 921 CD1 LEU 120 43.830 45.349 75.890 1.00 19.33 DIC ATOM 922 CD2 LEU 120 41.924 43.796 75.627 1.00 17.41 DIC ATOM 923 C LEU 120 43.457 44.333 80.303 1.00 19.39 DIC ATOM 924 O LEU 120 42.377 44.121 80.857 1.00 19.64 DIC ATOM 925 N GLY 121 44.611 43.908 80.804 1.00 19.06 DIC ATOM 926 CA GLY 121 44.618 43.151 82.044 1.00 19.45 DIC ATOM 927 C GLY 121 43.724 41.933 81.890 1.00 19.65 DIC ATOM 928 O GLY 121 43.805 41.225 80.884 1.00 19.83 DIC ATOM 929 N ASN 122 42.863 41.672 82.866 1.00 19.86 DIC ATOM 930 CA ASN 122 41.982 40.518 82.747 1.00 20.32 DIC ATOM 931 CB ASN 122 41.870 39.765 84.079 1.00 22.30 DIC ATOM 932 CG ASN 122 41.270 38.374 83.910 1.00 23.86 DIC ATOM 933 OD1 ASN 122 41.773 37.559 83.132 1.00 24.87 DIC ATOM 934 ND2 ASN 122 40.193 38.099 84.637 1.00 24.89 DIC ATOM 935 C ASN 122 40.597 40.944 82.271 1.00 19.00 DIC ATOM 936 O ASN 122 39.629 40.201 82.424 1.00 18.30 DIC ATOM 937 N ASN 123 40.507 42.149 81.707 1.00 17.37 DIC ATOM 938 CA ASN 123 39.238 42.651 81.186 1.00 16.29 DIC ATOM 939 CB ASN 123 39.313 44.147 80.858 1.00 15.93 DIC ATOM 940 CG ASN 123 39.347 45.014 82.090 1.00 16.95 DIC ATOM 941 OD1 ASN 123 40.344 45.684 82.366 1.00 17.08 DIC ATOM 942 ND2 ASN 123 38.257 45.013 82.839 1.00 16.13 DIC ATOM 943 C ASN 123 38.935 41.895 79.908 1.00 15.30 DIC ATOM 944 O ASN 123 39.842 41.387 79.253 1.00 15.35 DIC ATOM 945 N TRP 124 37.656 41.834 79.551 1.00 14.51 DIC ATOM 946 CA TRP 124 37.238 41.137 78.350 1.00 12.04 DIC ATOM 947 CB TRP 124 35.727 40.935 78.354 1.00 12.24 DIC ATOM 948 CG TRP 124 35.220 39.973 79.384 1.00 12.53 DIC ATOM 949 CD2 TRP 124 35.162 38.547 79.264 1.00 12.85 DIC ATOM 950 CE2 TRP 124 34.518 38.054 80.422 1.00 12.47 DIC ATOM 951 CE3 TRP 124 35.587 37.635 78.285 1.00 12.98 DIC ATOM 952 CD1 TRP 124 34.635 40.282 80.583 1.00 11.72 DIC ATOM 953 NE1 TRP 124 34.206 39.131 81.210 1.00 12.73 DIC ATOM 954 CZ2 TRP 124 34.285 36.689 80.627 1.00 13.82 DIC ATOM 955 CZ3 TRP 124 35.354 36.277 78.491 1.00 14.04 DIC ATOM 956 CH2 TRP 124 34.709 35.821 79.652 1.00 13.35 DIC ATOM 957 C TRP 124 37.628 41.904 77.094 1.00 11.46 DIC ATOM 958 O TRP 124 37.992 41.308 76.088 1.00 10.17 DIC ATOM 959 N LEU 125 37.558 43.227 77.158 1.00 10.45 DIC ATOM 960 CA LEU 125 37.898 44.035 76.000 1.00 11.28 DIC ATOM 961 CB LEU 125 36.841 43.844 74.903 1.00 11.69 DIC ATOM 962 CG LEU 125 35.439 44.448 75.080 1.00 12.44 DIC ATOM 963 CD1 LEU 125 34.499 43.821 74.070 1.00 12.81 DIC ATOM 964 CD2 LEU 125 34.910 44.193 76.465 1.00 13.63 DIC ATOM 965 C LEU 125 37.995 45.505 76.366 1.00 11.38 DIC ATOM 966 O LEU 125 37.713 45.897 77.500 1.00 11.51 DIC ATOM 967 N GLY 126 38.415 46.305 75.397 1.00 10.75 DIC ATOM 968 CA GLY 126 38.526 47.735 75.592 1.00 11.81 DIC ATOM 969 C GLY 126 37.590 48.359 74.577 1.00 11.37 DIC ATOM 970 O GLY 126 37.579 47.939 73.418 1.00 11.54 DIC ATOM 971 N ALA 127 36.804 49.345 74.998 1.00 10.41 DIC ATOM 972 CA ALA 127 35.860 50.006 74.095 1.00 8.96 DIC ATOM 973 CB ALA 127 34.577 49.190 74.008 1.00 8.65 DIC ATOM 974 C ALA 127 35.536 51.431 74.535 1.00 9.67 DIC ATOM 975 O ALA 127 35.735 51.795 75.701 1.00 7.21 DIC ATOM 976 N SER 128 35.039 52.240 73.599 1.00 9.58 DIC ATOM 977 CA SER 128 34.675 53.617 73.916 1.00 10.71 DIC ATOM 978 CB SER 128 34.895 54.538 72.711 1.00 10.39 DIC ATOM 979 OG SER 128 36.250 54.510 72.286 1.00 10.31 DIC ATOM 980 C SER 128 33.206 53.644 74.321 1.00 11.60 DIC ATOM 981 O SER 128 32.408 52.818 73.857 1.00 10.65 DIC ATOM 982 N ILE 129 32.859 54.597 75.179 1.00 11.17 DIC ATOM 983 CA ILE 129 31.496 54.744 75.675 1.00 11.89 DIC ATOM 984 CB ILE 129 31.484 55.693 76.909 1.00 12.55 DIC ATOM 985 CG2 ILE 129 30.059 55.997 77.348 1.00 11.82 DIC ATOM 986 CG1 ILE 129 32.269 55.040 78.049 1.00 13.27 DIC ATOM 987 CD ILE 129 32.567 55.968 79.199 1.00 14.30 DIC ATOM 988 C ILE 129 30.538 55.257 74.600 1.00 13.23 DIC ATOM 989 O ILE 129 30.913 56.068 73.746 1.00 13.13 DIC ATOM 990 N ASP 130 29.300 54.771 74.647 1.00 12.89 DIC ATOM 991 CA ASP 130 28.280 55.167 73.693 1.00 13.14 DIC ATOM 992 CB ASP 130 27.447 53.944 73.284 1.00 12.35 DIC ATOM 993 CG ASP 130 26.610 54.195 72.039 1.00 12.78 DIC ATOM 994 OD1 ASP 130 25.776 55.130 72.033 1.00 14.26 DIC ATOM 995 OD2 ASP 130 26.784 53.454 71.060 1.00 13.48 DIC ATOM 996 C ASP 130 27.379 56.215 74.340 1.00 13.29 DIC ATOM 997 O ASP 130 26.483 55.878 75.112 1.00 13.88 DIC ATOM 998 N LEU 131 27.626 57.483 74.027 1.00 14.55 DIC ATOM 999 CA LEU 131 26.843 58.597 74.574 1.00 14.53 DIC ATOM 1000 CB LEU 131 27.401 59.933 74.071 1.00 15.55 DIC ATOM 1001 CG LEU 131 28.630 60.539 74.752 1.00 16.42 DIC ATOM 1002 CD1 LEU 131 29.698 59.495 75.006 1.00 17.97 DIC ATOM 1003 CD2 LEU 131 29.161 61.654 73.872 1.00 16.87 DIC ATOM 1004 C LEU 131 25.364 58.516 74.215 1.00 14.67 DIC ATOM 1005 O LEU 131 24.496 58.874 75.016 1.00 14.54 DIC ATOM 1006 N PHE 132 25.083 58.059 73.002 1.00 13.83 DIC ATOM 1007 CA PHE 132 23.714 57.935 72.528 1.00 14.23 DIC ATOM 1008 CB PHE 132 23.722 57.462 71.070 1.00 14.97 DIC ATOM 1009 CG PHE 132 22.354 57.288 70.481 1.00 16.38 DIC ATOM 1010 CD1 PHE 132 21.728 56.044 70.494 1.00 17.39 DIC ATOM 1011 CD2 PHE 132 21.685 58.368 69.924 1.00 17.06 DIC ATOM 1012 CE1 PHE 132 20.456 55.877 69.961 1.00 17.85 DIC ATOM 1013 CE2 PHE 132 20.405 58.215 69.385 1.00 19.05 DIC ATOM 1014 CZ PHE 132 19.790 56.962 69.404 1.00 19.20 DIC ATOM 1015 C PHE 132 22.896 56.974 73.398 1.00 14.47 DIC ATOM 1016 O PHE 132 21.769 57.290 73.793 1.00 14.19 DIC ATOM 1017 N VAL 133 23.464 55.807 73.703 1.00 12.67 DIC ATOM 1018 CA VAL 133 22.757 54.829 74.523 1.00 13.81 DIC ATOM 1019 CB VAL 133 23.396 53.433 74.433 1.00 12.45 DIC ATOM 1020 CG1 VAL 133 22.658 52.469 75.359 1.00 13.71 DIC ATOM 1021 CG2 VAL 133 23.330 52.924 73.002 1.00 12.09 DIC ATOM 1022 C VAL 133 22.734 55.248 75.983 1.00 14.81 DIC ATOM 1023 O VAL 133 21.710 55.125 76.659 1.00 15.65 DIC ATOM 1024 N GLU 134 23.864 55.753 76.462 1.00 16.17 DIC ATOM 1025 CA GLU 134 23.987 56.184 77.845 1.00 17.03 DIC ATOM 1026 CB GLU 134 25.408 56.700 78.089 1.00 17.49 DIC ATOM 1027 CG GLU 134 25.763 56.880 79.553 1.00 20.47 DIC ATOM 1028 CD GLU 134 25.781 55.575 80.329 1.00 18.73 DIC ATOM 1029 OE1 GLU 134 25.626 55.635 81.556 1.00 20.44 DIC ATOM 1030 OE2 GLU 134 25.959 54.496 79.729 1.00 20.43 DIC ATOM 1031 C GLU 134 22.955 57.252 78.230 1.00 18.44 DIC ATOM 1032 O GLU 134 22.529 57.321 79.378 1.00 18.74 DIC ATOM 1033 N ARG 135 22.540 58.082 77.281 1.00 18.60 DIC ATOM 1034 CA ARG 135 21.560 59.115 77.594 1.00 20.63 DIC ATOM 1035 CB ARG 135 21.897 60.419 76.867 1.00 22.18 DIC ATOM 1036 CG ARG 135 21.810 60.353 75.362 1.00 25.33 DIC ATOM 1037 CD ARG 135 22.541 61.540 74.759 1.00 28.60 DIC ATOM 1038 NE ARG 135 21.996 62.820 75.204 1.00 30.75 DIC ATOM 1039 CZ ARG 135 20.972 63.444 74.626 1.00 31.82 DIC ATOM 1040 NH1 ARG 135 20.547 64.606 75.110 1.00 32.80 DIC ATOM 1041 NH2 ARG 135 20.379 62.917 73.560 1.00 32.31 DIC ATOM 1042 C ARG 135 20.140 58.682 77.261 1.00 20.30 DIC ATOM 1043 O ARG 135 19.215 59.488 77.293 1.00 20.01 DIC ATOM 1044 N GLN 136 19.975 57.408 76.928 1.00 20.15 DIC ATOM 1045 CA GLN 136 18.660 56.864 76.631 1.00 20.32 DIC ATOM 1046 CB GLN 136 18.789 55.671 75.688 1.00 20.65 DIC ATOM 1047 CG GLN 136 17.480 55.152 75.143 1.00 21.22 DIC ATOM 1048 CD GLN 136 17.681 53.987 74.193 1.00 22.55 DIC ATOM 1049 OE1 GLN 136 18.653 53.953 73.436 1.00 22.60 DIC ATOM 1050 NE2 GLN 136 16.757 53.031 74.218 1.00 22.18 DIC ATOM 1051 C GLN 136 18.143 56.411 77.993 1.00 21.14 DIC ATOM 1052 O GLN 136 18.358 55.271 78.397 1.00 19.68 DIC ATOM 1053 N GLU 137 17.480 57.326 78.698 1.00 22.64 DIC ATOM 1054 CA GLU 137 16.955 57.086 80.045 1.00 24.24 DIC ATOM 1055 CB GLU 137 15.856 58.113 80.369 1.00 27.33 DIC ATOM 1056 CG GLU 137 15.631 58.389 81.868 1.00 32.13 DIC ATOM 1057 CD GLU 137 15.115 57.184 82.658 1.00 34.75 DIC ATOM 1058 OE1 GLU 137 14.132 56.543 82.217 1.00 36.51 DIC ATOM 1059 OE2 GLU 137 15.684 56.884 83.735 1.00 35.95 DIC ATOM 1060 C GLU 137 16.428 55.688 80.342 1.00 22.27 DIC ATOM 1061 O GLU 137 15.508 55.194 79.687 1.00 23.05 DIC ATOM 1062 N GLY 138 17.029 55.058 81.346 1.00 21.87 DIC ATOM 1063 CA GLY 138 16.604 53.738 81.774 1.00 20.02 DIC ATOM 1064 C GLY 138 16.855 52.556 80.859 1.00 19.14 DIC ATOM 1065 O GLY 138 16.587 51.426 81.253 1.00 19.29 DIC ATOM 1066 N TYR 139 17.371 52.779 79.654 1.00 18.23 DIC ATOM 1067 CA TYR 139 17.605 51.643 78.762 1.00 17.46 DIC ATOM 1068 CB TYR 139 18.111 52.080 77.389 1.00 15.54 DIC ATOM 1069 CG TYR 139 18.398 50.877 76.513 1.00 14.37 DIC ATOM 1070 CD1 TYR 139 17.358 50.087 76.029 1.00 14.45 DIC ATOM 1071 CE1 TYR 139 17.604 48.932 75.298 1.00 14.12 DIC ATOM 1072 CD2 TYR 139 19.708 50.480 76.237 1.00 14.19 DIC ATOM 1073 CE2 TYR 139 19.969 49.313 75.503 1.00 13.62 DIC ATOM 1074 CZ TYR 139 18.910 48.547 75.039 1.00 13.67 DIC ATOM 1075 OH TYR 139 19.142 47.398 74.316 1.00 12.91 DIC ATOM 1076 C TYR 139 18.621 50.664 79.326 1.00 16.80 DIC ATOM 1077 O TYR 139 18.353 49.474 79.442 1.00 18.25 DIC ATOM 1078 N LYS 140 19.798 51.183 79.638 1.00 15.97 DIC ATOM 1079 CA LYS 140 20.905 50.398 80.166 1.00 16.47 DIC ATOM 1080 CB LYS 140 21.957 51.356 80.726 1.00 17.96 DIC ATOM 1081 CG LYS 140 23.344 50.799 80.841 1.00 18.12 DIC ATOM 1082 CD LYS 140 24.340 51.897 81.191 1.00 17.26 DIC ATOM 1083 CE LYS 140 24.014 52.584 82.505 1.00 18.38 DIC ATOM 1084 NZ LYS 140 25.094 53.524 82.900 1.00 18.19 DIC ATOM 1085 C LYS 140 20.443 49.427 81.244 1.00 17.24 DIC ATOM 1086 O LYS 140 20.853 48.264 81.264 1.00 16.57 DIC ATOM 1087 N GLN 141 19.579 49.907 82.134 1.00 16.44 DIC ATOM 1088 CA GLN 141 19.064 49.086 83.219 1.00 17.66 DIC ATOM 1089 CB GLN 141 18.298 49.958 84.220 1.00 17.58 DIC ATOM 1090 CG GLN 141 19.177 50.921 85.010 1.00 16.44 DIC ATOM 1091 CD GLN 141 19.667 52.100 84.183 1.00 18.00 DIC ATOM 1092 OE1 GLN 141 19.272 52.274 83.033 1.00 17.29 DIC ATOM 1093 NE2 GLN 141 20.525 52.920 84.772 1.00 17.45 DIC ATOM 1094 C GLN 141 18.176 47.941 82.730 1.00 17.85 DIC ATOM 1095 O GLN 141 18.076 46.902 83.384 1.00 18.70 DIC ATOM 1096 N LYS 142 17.534 48.130 81.582 1.00 18.33 DIC ATOM 1097 CA LYS 142 16.678 47.094 81.007 1.00 18.53 DIC ATOM 1098 CB LYS 142 15.989 47.600 79.736 1.00 20.13 DIC ATOM 1099 CG LYS 142 14.819 48.553 79.963 1.00 23.26 DIC ATOM 1100 CD LYS 142 14.382 49.182 78.639 1.00 24.62 DIC ATOM 1101 CE LYS 142 13.112 50.012 78.779 1.00 27.12 DIC ATOM 1102 NZ LYS 142 11.922 49.174 79.116 1.00 27.95 DIC ATOM 1103 C LYS 142 17.477 45.839 80.662 1.00 17.52 DIC ATOM 1104 O LYS 142 16.921 44.737 80.628 1.00 17.09 DIC ATOM 1105 N ILE 143 18.771 45.987 80.384 1.00 15.77 DIC ATOM 1106 CA ILE 143 19.561 44.802 80.054 1.00 13.94 DIC ATOM 1107 CB ILE 143 20.391 44.979 78.754 1.00 13.64 DIC ATOM 1108 CG2 ILE 143 19.467 45.307 77.584 1.00 13.27 DIC ATOM 1109 CG1 ILE 143 21.434 46.079 78.919 1.00 13.02 DIC ATOM 1110 CD ILE 143 22.390 46.147 77.731 1.00 13.03 DIC ATOM 1111 C ILE 143 20.472 44.349 81.193 1.00 13.33 DIC ATOM 1112 O ILE 143 21.480 43.679 80.974 1.00 12.63 DIC ATOM 1113 N GLY 144 20.099 44.722 82.415 1.00 13.50 DIC ATOM 1114 CA GLY 144 20.849 44.304 83.585 1.00 12.47 DIC ATOM 1115 C GLY 144 22.073 45.084 84.013 1.00 13.88 DIC ATOM 1116 O GLY 144 22.794 44.632 84.903 1.00 12.20 DIC ATOM 1117 N MSE 145 22.320 46.242 83.410 1.00 14.02 DIC ATOM 1118 CA MSE 145 23.487 47.028 83.789 1.00 15.34 DIC ATOM 1119 CB MSE 145 24.054 47.746 82.568 1.00 14.88 DIC ATOM 1120 CG MSE 145 24.544 46.810 81.471 1.00 14.27 DIC ATOM 1121 SE MSE 145 25.198 47.793 79.939 1.00 16.53 DIC ATOM 1122 CE MSE 145 26.784 48.563 80.704 1.00 12.51 DIC ATOM 1123 C MSE 145 23.166 48.045 84.882 1.00 16.35 DIC ATOM 1124 O MSE 145 22.033 48.516 84.996 1.00 16.93 DIC ATOM 1125 N ALA 146 24.168 48.379 85.687 1.00 17.18 DIC ATOM 1126 CA ALA 146 23.979 49.357 86.760 1.00 17.93 DIC ATOM 1127 CB ALA 146 24.876 49.016 87.947 1.00 19.51 DIC ATOM 1128 C ALA 146 24.304 50.753 86.235 1.00 18.51 DIC ATOM 1129 O ALA 146 24.880 50.892 85.156 1.00 16.64 DIC ATOM 1130 N ASP 147 23.929 51.782 86.995 1.00 18.52 DIC ATOM 1131 CA ASP 147 24.181 53.166 86.594 1.00 19.15 DIC ATOM 1132 CB ASP 147 23.589 54.143 87.622 1.00 22.16 DIC ATOM 1133 CG ASP 147 23.911 55.600 87.299 1.00 24.53 DIC ATOM 1134 OD1 ASP 147 23.468 56.101 86.245 1.00 27.39 DIC ATOM 1135 OD2 ASP 147 24.614 56.250 88.096 1.00 26.51 DIC ATOM 1136 C ASP 147 25.668 53.456 86.427 1.00 18.18 DIC ATOM 1137 O ASP 147 26.062 54.243 85.558 1.00 18.44 DIC ATOM 1138 N GLY 148 26.485 52.813 87.258 1.00 15.95 DIC ATOM 1139 CA GLY 148 27.920 53.015 87.207 1.00 14.91 DIC ATOM 1140 C GLY 148 28.645 52.201 86.152 1.00 14.80 DIC ATOM 1141 O GLY 148 29.858 52.324 85.996 1.00 14.63 DIC ATOM 1142 N GLU 149 27.912 51.360 85.430 1.00 13.75 DIC ATOM 1143 CA GLU 149 28.510 50.548 84.379 1.00 14.04 DIC ATOM 1144 CB GLU 149 27.953 49.121 84.424 1.00 13.92 DIC ATOM 1145 CG GLU 149 28.202 48.416 85.755 1.00 14.93 DIC ATOM 1146 CD GLU 149 27.689 46.989 85.769 1.00 14.83 DIC ATOM 1147 OE1 GLU 149 26.585 46.749 85.238 1.00 15.36 DIC ATOM 1148 OE2 GLU 149 28.383 46.109 86.320 1.00 14.29 DIC ATOM 1149 C GLU 149 28.150 51.237 83.067 1.00 13.46 DIC ATOM 1150 O GLU 149 26.980 51.361 82.716 1.00 13.23 DIC ATOM 1151 N TYR 150 29.165 51.695 82.349 1.00 12.32 DIC ATOM 1152 CA TYR 150 28.928 52.419 81.116 1.00 12.18 DIC ATOM 1153 CB TYR 150 30.023 53.470 80.961 1.00 12.48 DIC ATOM 1154 CG TYR 150 30.127 54.320 82.211 1.00 13.07 DIC ATOM 1155 CD1 TYR 150 31.351 54.526 82.833 1.00 12.79 DIC ATOM 1156 CE1 TYR 150 31.442 55.235 84.016 1.00 13.05 DIC ATOM 1157 CD2 TYR 150 28.984 54.860 82.807 1.00 12.92 DIC ATOM 1158 CE2 TYR 150 29.063 55.577 83.999 1.00 13.33 DIC ATOM 1159 CZ TYR 150 30.302 55.756 84.595 1.00 14.14 DIC ATOM 1160 OH TYR 150 30.417 56.439 85.775 1.00 13.21 DIC ATOM 1161 C TYR 150 28.786 51.562 79.870 1.00 10.46 DIC ATOM 1162 O TYR 150 29.604 50.681 79.603 1.00 9.61 DIC ATOM 1163 N TYR 151 27.720 51.839 79.126 1.00 9.17 DIC ATOM 1164 CA TYR 151 27.381 51.124 77.901 1.00 8.84 DIC ATOM 1165 CB TYR 151 25.949 51.469 77.502 1.00 8.39 DIC ATOM 1166 CG TYR 151 25.359 50.630 76.391 1.00 9.04 DIC ATOM 1167 CD1 TYR 151 25.744 50.817 75.065 1.00 8.73 DIC ATOM 1168 CE1 TYR 151 25.175 50.062 74.039 1.00 8.50 DIC ATOM 1169 CD2 TYR 151 24.387 49.666 76.668 1.00 8.78 DIC ATOM 1170 CE2 TYR 151 23.813 48.910 75.649 1.00 8.51 DIC ATOM 1171 CZ TYR 151 24.212 49.113 74.339 1.00 8.79 DIC ATOM 1172 OH TYR 151 23.650 48.364 73.331 1.00 6.56 DIC ATOM 1173 C TYR 151 28.346 51.519 76.797 1.00 7.98 DIC ATOM 1174 O TYR 151 28.461 52.697 76.456 1.00 8.75 DIC ATOM 1175 N PHE 152 29.048 50.538 76.239 1.00 7.59 DIC ATOM 1176 CA PHE 152 30.008 50.839 75.192 1.00 8.73 DIC ATOM 1177 CB PHE 152 31.315 50.076 75.426 1.00 9.12 DIC ATOM 1178 CG PHE 152 31.165 48.581 75.416 1.00 9.52 DIC ATOM 1179 CD1 PHE 152 31.025 47.870 76.605 1.00 10.37 DIC ATOM 1180 CD2 PHE 152 31.206 47.875 74.219 1.00 9.21 DIC ATOM 1181 CE1 PHE 152 30.933 46.470 76.601 1.00 10.52 DIC ATOM 1182 CE2 PHE 152 31.115 46.474 74.208 1.00 10.71 DIC ATOM 1183 CZ PHE 152 30.980 45.775 75.397 1.00 10.62 DIC ATOM 1184 C PHE 152 29.468 50.530 73.810 1.00 9.25 DIC ATOM 1185 O PHE 152 28.521 49.753 73.659 1.00 9.63 DIC ATOM 1186 N ASN 153 30.060 51.169 72.804 1.00 9.40 DIC ATOM 1187 CA ASN 153 29.661 50.955 71.422 1.00 8.94 DIC ATOM 1188 CB ASN 153 29.916 52.211 70.590 1.00 10.41 DIC ATOM 1189 CG ASN 153 29.541 52.025 69.136 1.00 10.47 DIC ATOM 1190 OD1 ASN 153 30.337 51.537 68.334 1.00 11.66 DIC ATOM 1191 ND2 ASN 153 28.312 52.391 68.794 1.00 11.08 DIC ATOM 1192 C ASN 153 30.492 49.795 70.910 1.00 8.26 DIC ATOM 1193 O ASN 153 31.691 49.724 71.174 1.00 6.77 DIC ATOM 1194 N ALA 154 29.856 48.885 70.180 1.00 7.02 DIC ATOM 1195 CA ALA 154 30.547 47.702 69.676 1.00 7.92 DIC ATOM 1196 CB ALA 154 29.551 46.551 69.529 1.00 6.96 DIC ATOM 1197 C ALA 154 31.300 47.902 68.365 1.00 7.01 DIC ATOM 1198 O ALA 154 31.819 46.938 67.795 1.00 7.48 DIC ATOM 1199 N GLY 155 31.376 49.143 67.901 1.00 6.72 DIC ATOM 1200 CA GLY 155 32.053 49.426 66.647 1.00 7.21 DIC ATOM 1201 C GLY 155 33.573 49.409 66.635 1.00 7.94 DIC ATOM 1202 O GLY 155 34.185 49.242 65.575 1.00 7.30 DIC ATOM 1203 N VAL 156 34.183 49.606 67.800 1.00 7.67 DIC ATOM 1204 CA VAL 156 35.634 49.604 67.930 1.00 6.73 DIC ATOM 1205 CB VAL 156 36.183 51.053 68.035 1.00 8.07 DIC ATOM 1206 CG1 VAL 156 37.705 51.044 68.190 1.00 8.55 DIC ATOM 1207 CG2 VAL 156 35.794 51.846 66.784 1.00 6.66 DIC ATOM 1208 C VAL 156 35.928 48.834 69.210 1.00 6.86 DIC ATOM 1209 O VAL 156 35.639 49.306 70.304 1.00 5.93 DIC ATOM 1210 N LEU 157 36.493 47.640 69.066 1.00 5.63 DIC ATOM 1211 CA LEU 157 36.789 46.791 70.215 1.00 6.45 DIC ATOM 1212 CB LEU 157 35.818 45.607 70.246 1.00 5.76 DIC ATOM 1213 CG LEU 157 34.328 45.916 70.075 1.00 5.74 DIC ATOM 1214 CD1 LEU 157 33.585 44.625 69.840 1.00 4.70 DIC ATOM 1215 CD2 LEU 157 33.783 46.662 71.291 1.00 3.22 DIC ATOM 1216 C LEU 157 38.195 46.231 70.244 1.00 7.54 DIC ATOM 1217 O LEU 157 38.614 45.559 69.301 1.00 8.36 DIC ATOM 1218 N LEU 158 38.927 46.509 71.320 1.00 8.42 DIC ATOM 1219 CA LEU 158 40.264 45.947 71.486 1.00 9.61 DIC ATOM 1220 CB LEU 158 41.177 46.886 72.285 1.00 10.49 DIC ATOM 1221 CG LEU 158 42.640 46.441 72.402 1.00 10.54 DIC ATOM 1222 CD1 LEU 158 43.281 46.378 71.022 1.00 11.43 DIC ATOM 1223 CD2 LEU 158 43.394 47.419 73.282 1.00 12.79 DIC ATOM 1224 C LEU 158 39.940 44.695 72.291 1.00 10.50 DIC ATOM 1225 O LEU 158 39.581 44.772 73.466 1.00 10.19 DIC ATOM 1226 N ILE 159 40.074 43.538 71.656 1.00 11.09 DIC ATOM 1227 CA ILE 159 39.703 42.284 72.287 1.00 11.44 DIC ATOM 1228 CB ILE 159 38.855 41.459 71.277 1.00 12.05 DIC ATOM 1229 CG2 ILE 159 38.540 40.069 71.821 1.00 11.71 DIC ATOM 1230 CG1 ILE 159 37.575 42.247 70.961 1.00 12.04 DIC ATOM 1231 CD ILE 159 36.693 41.637 69.916 1.00 13.91 DIC ATOM 1232 C ILE 159 40.817 41.422 72.877 1.00 12.11 DIC ATOM 1233 O ILE 159 41.846 41.179 72.253 1.00 10.85 DIC ATOM 1234 N ASN 160 40.594 40.974 74.108 1.00 12.74 DIC ATOM 1235 CA ASN 160 41.542 40.110 74.800 1.00 12.51 DIC ATOM 1236 CB ASN 160 41.325 40.243 76.309 1.00 12.70 DIC ATOM 1237 CG ASN 160 42.282 39.404 77.119 1.00 12.50 DIC ATOM 1238 OD1 ASN 160 42.920 38.492 76.600 1.00 12.15 DIC ATOM 1239 ND2 ASN 160 42.378 39.703 78.405 1.00 10.49 DIC ATOM 1240 C ASN 160 41.178 38.701 74.325 1.00 13.36 DIC ATOM 1241 O ASN 160 40.512 37.956 75.041 1.00 13.18 DIC ATOM 1242 N LEU 161 41.601 38.342 73.112 1.00 14.44 DIC ATOM 1243 CA LEU 161 41.266 37.032 72.552 1.00 15.68 DIC ATOM 1244 CB LEU 161 41.846 36.856 71.142 1.00 15.57 DIC ATOM 1245 CG LEU 161 40.891 37.070 69.962 1.00 17.77 DIC ATOM 1246 CD1 LEU 161 41.565 36.578 68.692 1.00 16.72 DIC ATOM 1247 CD2 LEU 161 39.576 36.321 70.180 1.00 16.73 DIC ATOM 1248 C LEU 161 41.696 35.858 73.407 1.00 16.42 DIC ATOM 1249 O LEU 161 40.977 34.865 73.500 1.00 15.59 DIC ATOM 1250 N LYS 162 42.877 35.955 74.007 1.00 17.58 DIC ATOM 1251 CA LYS 162 43.365 34.883 74.865 1.00 18.16 DIC ATOM 1252 CB LYS 162 44.683 35.297 75.528 1.00 20.45 DIC ATOM 1253 CG LYS 162 45.123 34.368 76.643 1.00 22.89 DIC ATOM 1254 CD LYS 162 46.599 34.511 76.971 1.00 24.41 DIC ATOM 1255 CE LYS 162 47.470 33.764 75.961 1.00 25.88 DIC ATOM 1256 NZ LYS 162 48.892 33.703 76.422 1.00 26.93 DIC ATOM 1257 C LYS 162 42.303 34.568 75.927 1.00 17.16 DIC ATOM 1258 O LYS 162 42.020 33.406 76.210 1.00 16.94 DIC ATOM 1259 N LYS 163 41.705 35.608 76.506 1.00 16.20 DIC ATOM 1260 CA LYS 163 40.670 35.407 77.514 1.00 13.83 DIC ATOM 1261 CB LYS 163 40.291 36.728 78.189 1.00 13.03 DIC ATOM 1262 CG LYS 163 39.242 36.563 79.297 1.00 13.52 DIC ATOM 1263 CD LYS 163 39.031 37.864 80.064 1.00 13.40 DIC ATOM 1264 CE LYS 163 37.998 37.714 81.172 1.00 13.29 DIC ATOM 1265 NZ LYS 163 38.407 36.647 82.124 1.00 16.98 DIC ATOM 1266 C LYS 163 39.428 34.792 76.877 1.00 13.30 DIC ATOM 1267 O LYS 163 38.870 33.826 77.394 1.00 13.39 DIC ATOM 1268 N TRP 164 38.995 35.352 75.751 1.00 12.69 DIC ATOM 1269 CA TRP 164 37.817 34.832 75.056 1.00 12.44 DIC ATOM 1270 CB TRP 164 37.608 35.582 73.743 1.00 11.58 DIC ATOM 1271 CG TRP 164 37.001 36.958 73.891 1.00 10.67 DIC ATOM 1272 CD2 TRP 164 36.032 37.560 73.025 1.00 10.33 DIC ATOM 1273 CE2 TRP 164 35.796 38.867 73.502 1.00 10.22 DIC ATOM 1274 CE3 TRP 164 35.341 37.119 71.886 1.00 10.89 DIC ATOM 1275 CD1 TRP 164 37.304 37.895 74.833 1.00 10.43 DIC ATOM 1276 NE1 TRP 164 36.584 39.048 74.607 1.00 9.98 DIC ATOM 1277 CZ2 TRP 164 34.896 39.743 72.880 1.00 10.17 DIC ATOM 1278 CZ3 TRP 164 34.446 37.989 71.270 1.00 9.91 DIC ATOM 1279 CH2 TRP 164 34.234 39.286 71.769 1.00 9.87 DIC ATOM 1280 C TRP 164 37.923 33.329 74.766 1.00 13.17 DIC ATOM 1281 O TRP 164 36.961 32.580 74.959 1.00 10.76 DIC ATOM 1282 N ARG 165 39.090 32.882 74.311 1.00 13.97 DIC ATOM 1283 CA ARG 165 39.248 31.473 73.984 1.00 15.74 DIC ATOM 1284 CB ARG 165 40.576 31.242 73.250 1.00 16.55 DIC ATOM 1285 CG ARG 165 40.579 31.829 71.833 1.00 17.08 DIC ATOM 1286 CD ARG 165 41.687 31.245 70.956 1.00 16.86 DIC ATOM 1287 NE ARG 165 43.006 31.584 71.473 1.00 17.35 DIC ATOM 1288 CZ ARG 165 43.679 32.678 71.144 1.00 16.72 DIC ATOM 1289 NH1 ARG 165 44.865 32.907 71.678 1.00 17.09 DIC ATOM 1290 NH2 ARG 165 43.177 33.528 70.259 1.00 17.44 DIC ATOM 1291 C ARG 165 39.099 30.534 75.180 1.00 16.13 DIC ATOM 1292 O ARG 165 38.938 29.332 75.008 1.00 16.33 DIC ATOM 1293 N ARG 166 39.124 31.086 76.389 1.00 16.52 DIC ATOM 1294 CA ARG 166 38.959 30.282 77.597 1.00 17.40 DIC ATOM 1295 CB ARG 166 39.581 30.988 78.803 1.00 18.34 DIC ATOM 1296 CG ARG 166 41.089 31.074 78.767 1.00 20.01 DIC ATOM 1297 CD ARG 166 41.598 31.993 79.856 1.00 21.20 DIC ATOM 1298 NE ARG 166 43.045 32.146 79.773 1.00 23.88 DIC ATOM 1299 CZ ARG 166 43.688 33.305 79.868 1.00 24.44 DIC ATOM 1300 NH1 ARG 166 43.015 34.436 80.051 1.00 24.80 DIC ATOM 1301 NH2 ARG 166 45.010 33.334 79.770 1.00 24.70 DIC ATOM 1302 C ARG 166 37.480 30.033 77.889 1.00 17.20 DIC ATOM 1303 O ARG 166 37.145 29.220 78.745 1.00 16.99 DIC ATOM 1304 N HIS 167 36.595 30.726 77.177 1.00 16.51 DIC ATOM 1305 CA HIS 167 35.164 30.572 77.403 1.00 15.83 DIC ATOM 1306 CB HIS 167 34.609 31.848 78.055 1.00 15.92 DIC ATOM 1307 CG HIS 167 35.323 32.253 79.311 1.00 16.65 DIC ATOM 1308 CD2 HIS 167 36.463 32.960 79.499 1.00 16.23 DIC ATOM 1309 ND1 HIS 167 34.866 31.924 80.570 1.00 15.62 DIC ATOM 1310 CE1 HIS 167 35.693 32.412 81.478 1.00 16.49 DIC ATOM 1311 NE2 HIS 167 36.670 33.046 80.854 1.00 15.49 DIC ATOM 1312 C HIS 167 34.397 30.288 76.106 1.00 15.86 DIC ATOM 1313 O HIS 167 34.953 30.360 75.005 1.00 16.09 DIC ATOM 1314 N ASP 168 33.118 29.956 76.248 1.00 14.42 DIC ATOM 1315 CA ASP 168 32.261 29.687 75.097 1.00 14.22 DIC ATOM 1316 CB ASP 168 31.425 28.416 75.310 1.00 13.99 DIC ATOM 1317 CG ASP 168 30.692 27.981 74.049 1.00 13.84 DIC ATOM 1318 OD1 ASP 168 30.323 26.791 73.944 1.00 14.98 DIC ATOM 1319 OD2 ASP 168 30.475 28.829 73.159 1.00 12.73 DIC ATOM 1320 C ASP 168 31.352 30.896 74.951 1.00 13.64 DIC ATOM 1321 O ASP 168 30.215 30.897 75.423 1.00 13.29 DIC ATOM 1322 N ILE 169 31.882 31.922 74.292 1.00 12.99 DIC ATOM 1323 CA ILE 169 31.187 33.188 74.070 1.00 12.79 DIC ATOM 1324 CB ILE 169 32.093 34.169 73.286 1.00 12.63 DIC ATOM 1325 CG2 ILE 169 31.461 35.565 73.260 1.00 12.96 DIC ATOM 1326 CG1 ILE 169 33.471 34.242 73.952 1.00 12.18 DIC ATOM 1327 CD ILE 169 33.437 34.760 75.384 1.00 12.46 DIC ATOM 1328 C ILE 169 29.848 33.051 73.342 1.00 12.16 DIC ATOM 1329 O ILE 169 28.882 33.745 73.671 1.00 11.43 DIC ATOM 1330 N PHE 170 29.785 32.157 72.361 1.00 12.91 DIC ATOM 1331 CA PHE 170 28.545 31.953 71.618 1.00 13.05 DIC ATOM 1332 CB PHE 170 28.789 31.044 70.407 1.00 13.59 DIC ATOM 1333 CG PHE 170 27.558 30.804 69.569 1.00 13.99 DIC ATOM 1334 CD1 PHE 170 26.952 29.549 69.536 1.00 15.41 DIC ATOM 1335 CD2 PHE 170 26.987 31.839 68.838 1.00 14.92 DIC ATOM 1336 CE1 PHE 170 25.782 29.327 68.779 1.00 16.57 DIC ATOM 1337 CE2 PHE 170 25.822 31.633 68.081 1.00 15.52 DIC ATOM 1338 CZ PHE 170 25.218 30.375 68.052 1.00 15.31 DIC ATOM 1339 C PHE 170 27.473 31.350 72.528 1.00 13.66 DIC ATOM 1340 O PHE 170 26.303 31.756 72.491 1.00 13.17 DIC ATOM 1341 N LYS 171 27.871 30.392 73.358 1.00 13.51 DIC ATOM 1342 CA LYS 171 26.927 29.761 74.267 1.00 14.35 DIC ATOM 1343 CB LYS 171 27.601 28.601 75.009 1.00 16.69 DIC ATOM 1344 CG LYS 171 26.639 27.736 75.820 1.00 19.33 DIC ATOM 1345 CD LYS 171 27.224 26.351 76.092 1.00 22.68 DIC ATOM 1346 CE LYS 171 27.426 25.569 74.799 1.00 24.24 DIC ATOM 1347 NZ LYS 171 28.095 24.259 75.028 1.00 27.40 DIC ATOM 1348 C LYS 171 26.422 30.826 75.243 1.00 13.97 DIC ATOM 1349 O LYS 171 25.219 30.987 75.429 1.00 13.72 DIC ATOM 1350 N MSE 172 27.346 31.565 75.846 1.00 12.85 DIC ATOM 1351 CA MSE 172 26.983 32.632 76.770 1.00 13.48 DIC ATOM 1352 CB MSE 172 28.248 33.312 77.300 1.00 14.61 DIC ATOM 1353 CG MSE 172 29.085 32.439 78.237 1.00 15.80 DIC ATOM 1354 SE MSE 172 30.883 33.124 78.407 1.00 17.35 DIC ATOM 1355 CE MSE 172 30.480 34.735 79.370 1.00 14.60 DIC ATOM 1356 C MSE 172 26.089 33.671 76.076 1.00 13.42 DIC ATOM 1357 O MSE 172 25.210 34.261 76.708 1.00 13.11 DIC ATOM 1358 N SER 173 26.317 33.890 74.781 1.00 11.96 DIC ATOM 1359 CA SER 173 25.529 34.862 74.013 1.00 12.42 DIC ATOM 1360 CB SER 173 26.161 35.115 72.641 1.00 12.29 DIC ATOM 1361 OG SER 173 27.392 35.813 72.743 1.00 11.94 DIC ATOM 1362 C SER 173 24.097 34.376 73.813 1.00 12.80 DIC ATOM 1363 O SER 173 23.137 35.135 73.994 1.00 12.03 DIC ATOM 1364 N SER 174 23.966 33.109 73.429 1.00 12.50 DIC ATOM 1365 CA SER 174 22.663 32.504 73.200 1.00 12.95 DIC ATOM 1366 CB SER 174 22.816 31.058 72.726 1.00 12.51 DIC ATOM 1367 OG SER 174 23.397 31.000 71.439 1.00 14.05 DIC ATOM 1368 C SER 174 21.825 32.531 74.467 1.00 13.04 DIC ATOM 1369 O SER 174 20.634 32.843 74.422 1.00 11.55 DIC ATOM 1370 N GLU 175 22.444 32.187 75.593 1.00 13.58 DIC ATOM 1371 CA GLU 175 21.734 32.178 76.862 1.00 13.73 DIC ATOM 1372 CB GLU 175 22.609 31.558 77.957 1.00 15.98 DIC ATOM 1373 CG GLU 175 23.177 30.204 77.547 1.00 18.50 DIC ATOM 1374 CD GLU 175 23.988 29.525 78.638 1.00 20.33 DIC ATOM 1375 OE1 GLU 175 24.647 30.230 79.434 1.00 20.34 DIC ATOM 1376 OE2 GLU 175 23.977 28.272 78.681 1.00 21.97 DIC ATOM 1377 C GLU 175 21.332 33.598 77.238 1.00 12.97 DIC ATOM 1378 O GLU 175 20.244 33.818 77.762 1.00 12.29 DIC ATOM 1379 N TRP 176 22.199 34.568 76.954 1.00 12.77 DIC ATOM 1380 CA TRP 176 21.880 35.955 77.276 1.00 13.08 DIC ATOM 1381 CB TRP 176 23.105 36.853 77.085 1.00 13.64 DIC ATOM 1382 CG TRP 176 22.948 38.199 77.725 1.00 12.77 DIC ATOM 1383 CD2 TRP 176 22.404 39.376 77.125 1.00 12.50 DIC ATOM 1384 CE2 TRP 176 22.415 40.390 78.107 1.00 13.44 DIC ATOM 1385 CE3 TRP 176 21.904 39.674 75.852 1.00 12.57 DIC ATOM 1386 CD1 TRP 176 23.261 38.537 79.011 1.00 14.02 DIC ATOM 1387 NE1 TRP 176 22.945 39.849 79.249 1.00 13.70 DIC ATOM 1388 CZ2 TRP 176 21.942 41.685 77.855 1.00 13.81 DIC ATOM 1389 CZ3 TRP 176 21.432 40.962 75.601 1.00 11.62 DIC ATOM 1390 CH2 TRP 176 21.456 41.949 76.598 1.00 13.55 DIC ATOM 1391 C TRP 176 20.732 36.450 76.394 1.00 13.25 DIC ATOM 1392 O TRP 176 19.836 37.154 76.866 1.00 13.29 DIC ATOM 1393 N VAL 177 20.761 36.085 75.114 1.00 13.68 DIC ATOM 1394 CA VAL 177 19.708 36.493 74.188 1.00 13.26 DIC ATOM 1395 CB VAL 177 20.012 36.021 72.750 1.00 12.93 DIC ATOM 1396 CG1 VAL 177 18.760 36.146 71.874 1.00 12.53 DIC ATOM 1397 CG2 VAL 177 21.128 36.862 72.155 1.00 12.01 DIC ATOM 1398 C VAL 177 18.378 35.906 74.649 1.00 15.29 DIC ATOM 1399 O VAL 177 17.327 36.554 74.580 1.00 14.53 DIC ATOM 1400 N GLU 178 18.428 34.676 75.139 1.00 16.30 DIC ATOM 1401 CA GLU 178 17.221 34.021 75.607 1.00 19.15 DIC ATOM 1402 CB GLU 178 17.537 32.573 76.001 1.00 21.26 DIC ATOM 1403 CG GLU 178 16.313 31.704 76.275 1.00 25.37 DIC ATOM 1404 CD GLU 178 15.292 31.740 75.144 1.00 26.83 DIC ATOM 1405 OE1 GLU 178 15.687 31.622 73.960 1.00 28.31 DIC ATOM 1406 OE2 GLU 178 14.087 31.883 75.445 1.00 28.46 DIC ATOM 1407 C GLU 178 16.656 34.792 76.798 1.00 18.93 DIC ATOM 1408 O GLU 178 15.442 34.896 76.964 1.00 19.05 DIC ATOM 1409 N GLN 179 17.544 35.360 77.605 1.00 18.25 DIC ATOM 1410 CA GLN 179 17.141 36.105 78.790 1.00 20.06 DIC ATOM 1411 CB GLN 179 18.308 36.134 79.784 1.00 21.74 DIC ATOM 1412 CG GLN 179 18.013 36.801 81.119 1.00 25.00 DIC ATOM 1413 CD GLN 179 19.274 37.041 81.937 1.00 27.00 DIC ATOM 1414 OE1 GLN 179 19.221 37.576 83.050 1.00 29.16 DIC ATOM 1415 NE2 GLN 179 20.416 36.651 81.386 1.00 27.67 DIC ATOM 1416 C GLN 179 16.655 37.536 78.538 1.00 19.68 DIC ATOM 1417 O GLN 179 15.815 38.044 79.279 1.00 19.99 DIC ATOM 1418 N TYR 180 17.178 38.189 77.503 1.00 19.03 DIC ATOM 1419 CA TYR 180 16.799 39.570 77.217 1.00 18.49 DIC ATOM 1420 CB TYR 180 18.011 40.483 77.409 1.00 17.86 DIC ATOM 1421 CG TYR 180 18.475 40.591 78.840 1.00 16.21 DIC ATOM 1422 CD1 TYR 180 19.408 39.703 79.362 1.00 16.33 DIC ATOM 1423 CE1 TYR 180 19.840 39.811 80.679 1.00 16.04 DIC ATOM 1424 CD2 TYR 180 17.979 41.586 79.672 1.00 15.98 DIC ATOM 1425 CE2 TYR 180 18.400 41.698 80.988 1.00 15.72 DIC ATOM 1426 CZ TYR 180 19.330 40.812 81.485 1.00 15.22 DIC ATOM 1427 OH TYR 180 19.755 40.931 82.789 1.00 16.65 DIC ATOM 1428 C TYR 180 16.215 39.824 75.831 1.00 19.02 DIC ATOM 1429 O TYR 180 16.109 40.972 75.409 1.00 18.33 DIC ATOM 1430 N LYS 181 15.837 38.760 75.132 1.00 19.32 DIC ATOM 1431 CA LYS 181 15.291 38.879 73.785 1.00 20.45 DIC ATOM 1432 CB LYS 181 14.848 37.496 73.299 1.00 21.34 DIC ATOM 1433 CG LYS 181 14.196 37.475 71.922 1.00 24.95 DIC ATOM 1434 CD LYS 181 15.149 37.926 70.818 1.00 26.37 DIC ATOM 1435 CE LYS 181 14.466 37.879 69.456 1.00 27.47 DIC ATOM 1436 NZ LYS 181 14.072 36.492 69.067 1.00 29.43 DIC ATOM 1437 C LYS 181 14.133 39.870 73.619 1.00 20.56 DIC ATOM 1438 O LYS 181 14.045 40.560 72.608 1.00 21.00 DIC ATOM 1439 N ASP 182 13.253 39.947 74.610 1.00 20.10 DIC ATOM 1440 CA ASP 182 12.088 40.823 74.519 1.00 20.96 DIC ATOM 1441 CB ASP 182 10.964 40.275 75.402 1.00 21.98 DIC ATOM 1442 CG ASP 182 10.374 38.968 74.873 1.00 23.22 DIC ATOM 1443 OD1 ASP 182 9.574 38.346 75.602 1.00 24.34 DIC ATOM 1444 OD2 ASP 182 10.691 38.560 73.734 1.00 24.33 DIC ATOM 1445 C ASP 182 12.334 42.288 74.881 1.00 20.33 DIC ATOM 1446 O ASP 182 11.398 43.086 74.906 1.00 20.87 DIC ATOM 1447 N VAL 183 13.580 42.652 75.151 1.00 18.31 DIC ATOM 1448 CA VAL 183 13.866 44.023 75.532 1.00 17.11 DIC ATOM 1449 CB VAL 183 14.052 44.116 77.064 1.00 17.36 DIC ATOM 1450 CG1 VAL 183 15.351 43.427 77.482 1.00 15.90 DIC ATOM 1451 CG2 VAL 183 14.031 45.558 77.501 1.00 18.60 DIC ATOM 1452 C VAL 183 15.091 44.619 74.843 1.00 16.46 DIC ATOM 1453 O VAL 183 15.213 45.836 74.743 1.00 15.97 DIC ATOM 1454 N MSE 184 16.002 43.775 74.370 1.00 15.66 DIC ATOM 1455 CA MSE 184 17.195 44.292 73.714 1.00 14.63 DIC ATOM 1456 CB MSE 184 18.193 43.153 73.422 1.00 15.84 DIC ATOM 1457 CG MSE 184 17.673 41.995 72.601 1.00 15.47 DIC ATOM 1458 SE MSE 184 18.875 40.472 72.749 1.00 16.06 DIC ATOM 1459 CE MSE 184 20.077 40.875 71.295 1.00 14.11 DIC ATOM 1460 C MSE 184 16.816 45.053 72.448 1.00 14.45 DIC ATOM 1461 O MSE 184 15.944 44.623 71.683 1.00 13.76 DIC ATOM 1462 N GLN 185 17.456 46.203 72.248 1.00 12.74 DIC ATOM 1463 CA GLN 185 17.183 47.050 71.094 1.00 11.64 DIC ATOM 1464 CB GLN 185 16.728 48.438 71.565 1.00 13.80 DIC ATOM 1465 CG GLN 185 15.491 48.436 72.469 1.00 12.21 DIC ATOM 1466 CD GLN 185 15.125 49.825 72.981 1.00 13.45 DIC ATOM 1467 OE1 GLN 185 15.701 50.831 72.565 1.00 12.43 DIC ATOM 1468 NE2 GLN 185 14.159 49.881 73.888 1.00 12.29 DIC ATOM 1469 C GLN 185 18.406 47.211 70.198 1.00 12.26 DIC ATOM 1470 O GLN 185 18.299 47.714 69.072 1.00 10.28 DIC ATOM 1471 N TYR 186 19.571 46.784 70.680 1.00 10.35 DIC ATOM 1472 CA TYR 186 20.773 46.965 69.884 1.00 11.71 DIC ATOM 1473 CB TYR 186 21.709 47.965 70.579 1.00 11.81 DIC ATOM 1474 CG TYR 186 21.052 49.319 70.763 1.00 13.33 DIC ATOM 1475 CD1 TYR 186 20.566 49.720 72.007 1.00 13.33 DIC ATOM 1476 CE1 TYR 186 19.883 50.927 72.160 1.00 13.45 DIC ATOM 1477 CD2 TYR 186 20.844 50.165 69.669 1.00 14.56 DIC ATOM 1478 CE2 TYR 186 20.161 51.371 69.809 1.00 14.44 DIC ATOM 1479 CZ TYR 186 19.683 51.745 71.059 1.00 14.43 DIC ATOM 1480 OH TYR 186 19.010 52.937 71.204 1.00 12.04 DIC ATOM 1481 C TYR 186 21.535 45.725 69.441 1.00 10.15 DIC ATOM 1482 O TYR 186 22.730 45.791 69.167 1.00 10.75 DIC ATOM 1483 N GLN 187 20.829 44.603 69.376 1.00 8.94 DIC ATOM 1484 CA GLN 187 21.379 43.349 68.878 1.00 8.88 DIC ATOM 1485 CB GLN 187 21.399 43.447 67.342 1.00 9.31 DIC ATOM 1486 CG GLN 187 19.987 43.785 66.826 1.00 10.51 DIC ATOM 1487 CD GLN 187 19.891 44.176 65.360 1.00 10.67 DIC ATOM 1488 OE1 GLN 187 18.788 44.374 64.849 1.00 12.93 DIC ATOM 1489 NE2 GLN 187 21.021 44.303 64.684 1.00 10.73 DIC ATOM 1490 C GLN 187 22.726 42.898 69.458 1.00 8.99 DIC ATOM 1491 O GLN 187 22.833 42.742 70.671 1.00 9.41 DIC ATOM 1492 N ASP 188 23.742 42.675 68.618 1.00 8.46 DIC ATOM 1493 CA ASP 188 25.040 42.207 69.112 1.00 9.37 DIC ATOM 1494 CB ASP 188 26.017 41.980 67.951 1.00 10.94 DIC ATOM 1495 CG ASP 188 26.258 43.231 67.147 1.00 11.67 DIC ATOM 1496 OD1 ASP 188 25.359 43.619 66.370 1.00 12.99 DIC ATOM 1497 OD2 ASP 188 27.340 43.832 67.298 1.00 12.63 DIC ATOM 1498 C ASP 188 25.692 43.140 70.131 1.00 9.34 DIC ATOM 1499 O ASP 188 26.444 42.707 71.006 1.00 8.86 DIC ATOM 1500 N GLN 189 25.393 44.422 70.020 1.00 8.62 DIC ATOM 1501 CA GLN 189 25.955 45.401 70.928 1.00 9.00 DIC ATOM 1502 CB GLN 189 25.620 46.803 70.419 1.00 8.38 DIC ATOM 1503 CG GLN 189 26.246 47.941 71.193 1.00 8.88 DIC ATOM 1504 CD GLN 189 26.110 49.255 70.445 1.00 9.01 DIC ATOM 1505 OE1 GLN 189 27.025 49.673 69.730 1.00 10.27 DIC ATOM 1506 NE2 GLN 189 24.953 49.898 70.583 1.00 7.31 DIC ATOM 1507 C GLN 189 25.406 45.165 72.337 1.00 9.05 DIC ATOM 1508 O GLN 189 26.139 45.269 73.318 1.00 8.94 DIC ATOM 1509 N ASP 190 24.118 44.841 72.438 1.00 9.37 DIC ATOM 1510 CA ASP 190 23.527 44.569 73.739 1.00 9.91 DIC ATOM 1511 CB ASP 190 22.029 44.301 73.623 1.00 9.65 DIC ATOM 1512 CG ASP 190 21.222 45.563 73.412 1.00 10.87 DIC ATOM 1513 OD1 ASP 190 20.179 45.475 72.740 1.00 8.70 DIC ATOM 1514 OD2 ASP 190 21.618 46.632 73.928 1.00 10.04 DIC ATOM 1515 C ASP 190 24.196 43.346 74.341 1.00 9.18 DIC ATOM 1516 O ASP 190 24.581 43.365 75.497 1.00 10.40 DIC ATOM 1517 N ILE 191 24.331 42.284 73.554 1.00 9.00 DIC ATOM 1518 CA ILE 191 24.951 41.056 74.042 1.00 8.87 DIC ATOM 1519 CB ILE 191 25.086 40.023 72.917 1.00 8.34 DIC ATOM 1520 CG2 ILE 191 25.767 38.761 73.448 1.00 7.88 DIC ATOM 1521 CG1 ILE 191 23.699 39.689 72.363 1.00 8.24 DIC ATOM 1522 CD ILE 191 23.732 38.844 71.104 1.00 7.49 DIC ATOM 1523 C ILE 191 26.327 41.283 74.662 1.00 9.65 DIC ATOM 1524 O ILE 191 26.589 40.839 75.783 1.00 9.14 DIC ATOM 1525 N LEU 192 27.201 41.979 73.936 1.00 9.83 DIC ATOM 1526 CA LEU 192 28.550 42.260 74.413 1.00 9.59 DIC ATOM 1527 CB LEU 192 29.331 43.055 73.362 1.00 9.02 DIC ATOM 1528 CG LEU 192 29.555 42.376 72.012 1.00 8.81 DIC ATOM 1529 CD1 LEU 192 30.078 43.409 71.009 1.00 7.76 DIC ATOM 1530 CD2 LEU 192 30.530 41.225 72.167 1.00 9.35 DIC ATOM 1531 C LEU 192 28.538 43.030 75.733 1.00 9.85 DIC ATOM 1532 O LEU 192 29.276 42.695 76.656 1.00 9.13 DIC ATOM 1533 N ASN 193 27.706 44.062 75.823 1.00 9.48 DIC ATOM 1534 CA ASN 193 27.612 44.850 77.052 1.00 9.51 DIC ATOM 1535 CB ASN 193 26.676 46.045 76.849 1.00 9.70 DIC ATOM 1536 CG ASN 193 27.394 47.256 76.290 1.00 10.74 DIC ATOM 1537 OD1 ASN 193 28.041 47.996 77.033 1.00 8.96 DIC ATOM 1538 ND2 ASN 193 27.297 47.461 74.972 1.00 10.60 DIC ATOM 1539 C ASN 193 27.102 44.011 78.221 1.00 9.96 DIC ATOM 1540 O ASN 193 27.620 44.109 79.334 1.00 9.61 DIC ATOM 1541 N GLY 194 26.079 43.199 77.963 1.00 10.54 DIC ATOM 1542 CA GLY 194 25.513 42.369 79.011 1.00 11.12 DIC ATOM 1543 C GLY 194 26.479 41.326 79.532 1.00 11.80 DIC ATOM 1544 O GLY 194 26.612 41.139 80.746 1.00 11.37 DIC ATOM 1545 N LEU 195 27.162 40.643 78.618 1.00 11.19 DIC ATOM 1546 CA LEU 195 28.111 39.605 79.004 1.00 10.80 DIC ATOM 1547 CB LEU 195 28.557 38.788 77.785 1.00 7.99 DIC ATOM 1548 CG LEU 195 27.589 37.864 77.048 1.00 7.39 DIC ATOM 1549 CD1 LEU 195 28.334 37.170 75.910 1.00 6.05 DIC ATOM 1550 CD2 LEU 195 27.021 36.821 78.012 1.00 6.98 DIC ATOM 1551 C LEU 195 29.370 40.111 79.702 1.00 11.37 DIC ATOM 1552 O LEU 195 29.864 39.464 80.623 1.00 11.30 DIC ATOM 1553 N PHE 196 29.889 41.259 79.271 1.00 11.32 DIC ATOM 1554 CA PHE 196 31.143 41.763 79.831 1.00 11.00 DIC ATOM 1555 CB PHE 196 32.106 42.123 78.690 1.00 10.77 DIC ATOM 1556 CG PHE 196 32.297 41.017 77.689 1.00 11.74 DIC ATOM 1557 CD1 PHE 196 32.353 39.690 78.102 1.00 10.22 DIC ATOM 1558 CD2 PHE 196 32.445 41.302 76.339 1.00 10.79 DIC ATOM 1559 CE1 PHE 196 32.560 38.658 77.184 1.00 11.95 DIC ATOM 1560 CE2 PHE 196 32.649 40.278 75.411 1.00 11.65 DIC ATOM 1561 CZ PHE 196 32.708 38.955 75.836 1.00 11.34 DIC ATOM 1562 C PHE 196 31.103 42.923 80.812 1.00 11.21 DIC ATOM 1563 O PHE 196 32.154 43.356 81.280 1.00 10.49 DIC ATOM 1564 N LYS 197 29.912 43.428 81.119 1.00 11.58 DIC ATOM 1565 CA LYS 197 29.773 44.544 82.050 1.00 11.43 DIC ATOM 1566 CB LYS 197 28.291 44.737 82.417 1.00 11.39 DIC ATOM 1567 CG LYS 197 27.594 43.539 83.091 1.00 12.71 DIC ATOM 1568 CD LYS 197 26.097 43.828 83.262 1.00 11.95 DIC ATOM 1569 CE LYS 197 25.351 42.749 84.053 1.00 12.18 DIC ATOM 1570 NZ LYS 197 25.288 41.442 83.336 1.00 10.84 DIC ATOM 1571 C LYS 197 30.612 44.304 83.305 1.00 12.30 DIC ATOM 1572 O LYS 197 30.632 43.199 83.846 1.00 11.29 DIC ATOM 1573 N GLY 198 31.321 45.333 83.758 1.00 12.29 DIC ATOM 1574 CA GLY 198 32.153 45.182 84.942 1.00 13.17 DIC ATOM 1575 C GLY 198 33.546 44.680 84.614 1.00 13.23 DIC ATOM 1576 O GLY 198 34.450 44.733 85.453 1.00 12.63 DIC ATOM 1577 N GLY 199 33.718 44.184 83.390 1.00 13.28 DIC ATOM 1578 CA GLY 199 35.011 43.688 82.952 1.00 13.74 DIC ATOM 1579 C GLY 199 35.387 44.341 81.628 1.00 14.37 DIC ATOM 1580 O GLY 199 35.845 43.680 80.696 1.00 13.49 DIC ATOM 1581 N VAL 200 35.176 45.651 81.560 1.00 13.59 DIC ATOM 1582 CA VAL 200 35.468 46.446 80.374 1.00 14.48 DIC ATOM 1583 CB VAL 200 34.172 47.103 79.823 1.00 14.24 DIC ATOM 1584 CG1 VAL 200 34.506 48.063 78.700 1.00 16.87 DIC ATOM 1585 CG2 VAL 200 33.206 46.040 79.332 1.00 15.73 DIC ATOM 1586 C VAL 200 36.455 47.578 80.678 1.00 14.42 DIC ATOM 1587 O VAL 200 36.314 48.282 81.673 1.00 14.37 DIC ATOM 1588 N CYS 201 37.451 47.737 79.813 1.00 14.62 DIC ATOM 1589 CA CYS 201 38.426 48.814 79.935 1.00 15.36 DIC ATOM 1590 CB CYS 201 39.797 48.346 79.445 1.00 17.87 DIC ATOM 1591 SG CYS 201 41.042 49.652 79.343 1.00 24.36 DIC ATOM 1592 C CYS 201 37.877 49.890 79.005 1.00 14.95 DIC ATOM 1593 O CYS 201 37.561 49.599 77.856 1.00 14.31 DIC ATOM 1594 N TYR 202 37.729 51.122 79.479 1.00 14.76 DIC ATOM 1595 CA TYR 202 37.184 52.146 78.598 1.00 14.81 DIC ATOM 1596 CB TYR 202 36.228 53.076 79.346 1.00 16.13 DIC ATOM 1597 CG TYR 202 35.108 52.377 80.083 1.00 16.70 DIC ATOM 1598 CD1 TYR 202 35.199 52.148 81.455 1.00 16.70 DIC ATOM 1599 CE1 TYR 202 34.166 51.540 82.156 1.00 17.89 DIC ATOM 1600 CD2 TYR 202 33.948 51.967 79.418 1.00 17.16 DIC ATOM 1601 CE2 TYR 202 32.900 51.347 80.113 1.00 17.82 DIC ATOM 1602 CZ TYR 202 33.020 51.143 81.486 1.00 18.36 DIC ATOM 1603 OH TYR 202 31.997 50.566 82.208 1.00 18.52 DIC ATOM 1604 C TYR 202 38.264 52.974 77.923 1.00 14.97 DIC ATOM 1605 O TYR 202 39.193 53.447 78.571 1.00 15.35 DIC ATOM 1606 N ALA 203 38.128 53.132 76.609 1.00 13.97 DIC ATOM 1607 CA ALA 203 39.068 53.902 75.801 1.00 13.45 DIC ATOM 1608 CB ALA 203 39.284 53.210 74.463 1.00 14.46 DIC ATOM 1609 C ALA 203 38.490 55.293 75.579 1.00 12.66 DIC ATOM 1610 O ALA 203 37.290 55.495 75.748 1.00 12.27 DIC ATOM 1611 N ASN 204 39.331 56.252 75.201 1.00 11.38 DIC ATOM 1612 CA ASN 204 38.856 57.612 74.964 1.00 10.72 DIC ATOM 1613 CB ASN 204 40.036 58.556 74.754 1.00 11.13 DIC ATOM 1614 CG ASN 204 39.620 59.996 74.762 1.00 10.71 DIC ATOM 1615 OD1 ASN 204 39.380 60.578 75.827 1.00 12.74 DIC ATOM 1616 ND2 ASN 204 39.503 60.584 73.578 1.00 10.78 DIC ATOM 1617 C ASN 204 37.945 57.645 73.734 1.00 10.83 DIC ATOM 1618 O ASN 204 38.100 56.833 72.815 1.00 9.54 DIC ATOM 1619 N SER 205 37.006 58.587 73.701 1.00 9.57 DIC ATOM 1620 CA SER 205 36.088 58.668 72.569 1.00 10.79 DIC ATOM 1621 CB SER 205 34.931 59.621 72.891 1.00 10.23 DIC ATOM 1622 OG SER 205 34.046 59.008 73.826 1.00 7.16 DIC ATOM 1623 C SER 205 36.740 59.052 71.251 1.00 10.81 DIC ATOM 1624 O SER 205 36.094 59.018 70.197 1.00 11.42 DIC ATOM 1625 N ARG 206 38.022 59.400 71.293 1.00 10.42 DIC ATOM 1626 CA ARG 206 38.728 59.759 70.064 1.00 10.38 DIC ATOM 1627 CB ARG 206 40.122 60.324 70.392 1.00 10.54 DIC ATOM 1628 CG ARG 206 41.103 59.329 70.992 1.00 11.01 DIC ATOM 1629 CD ARG 206 42.438 60.012 71.352 1.00 10.35 DIC ATOM 1630 NE ARG 206 42.972 60.735 70.200 1.00 11.14 DIC ATOM 1631 CZ ARG 206 44.020 60.350 69.477 1.00 9.85 DIC ATOM 1632 NH1 ARG 206 44.684 59.240 69.783 1.00 9.03 DIC ATOM 1633 NH2 ARG 206 44.389 61.069 68.426 1.00 7.77 DIC ATOM 1634 C ARG 206 38.854 58.508 69.188 1.00 9.72 DIC ATOM 1635 O ARG 206 39.059 58.593 67.973 1.00 8.91 DIC ATOM 1636 N PHE 207 38.719 57.341 69.812 1.00 9.74 DIC ATOM 1637 CA PHE 207 38.834 56.079 69.090 1.00 10.15 DIC ATOM 1638 CB PHE 207 39.583 55.053 69.947 1.00 10.78 DIC ATOM 1639 CG PHE 207 41.017 55.423 70.194 1.00 10.31 DIC ATOM 1640 CD1 PHE 207 41.452 55.792 71.465 1.00 10.66 DIC ATOM 1641 CD2 PHE 207 41.923 55.472 69.137 1.00 10.73 DIC ATOM 1642 CE1 PHE 207 42.771 56.215 71.674 1.00 10.88 DIC ATOM 1643 CE2 PHE 207 43.234 55.888 69.331 1.00 10.86 DIC ATOM 1644 CZ PHE 207 43.661 56.263 70.605 1.00 11.25 DIC ATOM 1645 C PHE 207 37.494 55.518 68.624 1.00 9.68 DIC ATOM 1646 O PHE 207 37.411 54.387 68.144 1.00 10.10 DIC ATOM 1647 N ASN 208 36.445 56.315 68.783 1.00 8.88 DIC ATOM 1648 CA ASN 208 35.114 55.936 68.335 1.00 9.98 DIC ATOM 1649 CB ASN 208 34.513 54.832 69.205 1.00 8.57 DIC ATOM 1650 CG ASN 208 33.371 54.116 68.507 1.00 7.87 DIC ATOM 1651 OD1 ASN 208 32.827 54.625 67.530 1.00 7.69 DIC ATOM 1652 ND2 ASN 208 33.002 52.939 69.000 1.00 6.25 DIC ATOM 1653 C ASN 208 34.253 57.188 68.397 1.00 10.42 DIC ATOM 1654 O ASN 208 33.368 57.316 69.240 1.00 11.59 DIC ATOM 1655 N PHE 209 34.532 58.109 67.482 1.00 10.12 DIC ATOM 1656 CA PHE 209 33.841 59.385 67.405 1.00 10.68 DIC ATOM 1657 CB PHE 209 34.788 60.421 66.784 1.00 10.56 DIC ATOM 1658 CG PHE 209 34.392 61.853 67.036 1.00 10.98 DIC ATOM 1659 CD1 PHE 209 34.475 62.401 68.311 1.00 12.28 DIC ATOM 1660 CD2 PHE 209 33.969 62.662 65.990 1.00 12.06 DIC ATOM 1661 CE1 PHE 209 34.141 63.742 68.545 1.00 12.45 DIC ATOM 1662 CE2 PHE 209 33.633 63.996 66.206 1.00 11.37 DIC ATOM 1663 CZ PHE 209 33.720 64.540 67.488 1.00 12.90 DIC ATOM 1664 C PHE 209 32.596 59.212 66.540 1.00 10.70 DIC ATOM 1665 O PHE 209 32.687 59.137 65.323 1.00 10.09 DIC ATOM 1666 N MSE 210 31.433 59.156 67.174 1.00 11.63 DIC ATOM 1667 CA MSE 210 30.178 58.963 66.446 1.00 12.51 DIC ATOM 1668 CB MSE 210 29.380 57.850 67.136 1.00 13.04 DIC ATOM 1669 CG MSE 210 30.140 56.526 67.190 1.00 12.66 DIC ATOM 1670 SE MSE 210 29.418 55.246 68.442 1.00 12.85 DIC ATOM 1671 CE MSE 210 30.266 55.875 70.045 1.00 11.55 DIC ATOM 1672 C MSE 210 29.364 60.253 66.363 1.00 12.05 DIC ATOM 1673 O MSE 210 29.735 61.265 66.958 1.00 12.49 DIC ATOM 1674 N PRO 211 28.245 60.240 65.613 1.00 12.41 DIC ATOM 1675 CD PRO 211 27.699 59.141 64.800 1.00 11.47 DIC ATOM 1676 CA PRO 211 27.408 61.439 65.482 1.00 11.06 DIC ATOM 1677 CB PRO 211 26.163 60.907 64.784 1.00 11.44 DIC ATOM 1678 CG PRO 211 26.732 59.865 63.882 1.00 11.64 DIC ATOM 1679 C PRO 211 27.074 62.121 66.817 1.00 11.44 DIC ATOM 1680 O PRO 211 27.073 63.355 66.915 1.00 11.07 DIC ATOM 1681 N THR 212 26.792 61.328 67.844 1.00 9.80 DIC ATOM 1682 CA THR 212 26.457 61.907 69.140 1.00 10.60 DIC ATOM 1683 CB THR 212 25.852 60.838 70.097 1.00 10.93 DIC ATOM 1684 OG1 THR 212 24.707 60.240 69.476 1.00 10.74 DIC ATOM 1685 CG2 THR 212 25.379 61.488 71.403 1.00 11.50 DIC ATOM 1686 C THR 212 27.656 62.609 69.798 1.00 11.02 DIC ATOM 1687 O THR 212 27.480 63.613 70.499 1.00 10.65 DIC ATOM 1688 N ASN 213 28.869 62.100 69.574 1.00 10.18 DIC ATOM 1689 CA ASN 213 30.064 62.725 70.148 1.00 10.69 DIC ATOM 1690 CB ASN 213 31.316 61.878 69.884 1.00 9.50 DIC ATOM 1691 CG ASN 213 31.212 60.462 70.459 1.00 8.75 DIC ATOM 1692 OD1 ASN 213 31.624 60.196 71.595 1.00 9.99 DIC ATOM 1693 ND2 ASN 213 30.651 59.556 69.677 1.00 5.77 DIC ATOM 1694 C ASN 213 30.229 64.083 69.482 1.00 12.35 DIC ATOM 1695 O ASN 213 30.591 65.068 70.130 1.00 12.36 DIC ATOM 1696 N TYR 214 29.961 64.128 68.180 1.00 12.87 DIC ATOM 1697 CA TYR 214 30.075 65.365 67.429 1.00 15.87 DIC ATOM 1698 CB TYR 214 29.837 65.117 65.940 1.00 17.04 DIC ATOM 1699 CG TYR 214 29.964 66.370 65.106 1.00 19.24 DIC ATOM 1700 CD1 TYR 214 31.212 66.888 64.777 1.00 19.84 DIC ATOM 1701 CE1 TYR 214 31.335 68.067 64.043 1.00 21.17 DIC ATOM 1702 CD2 TYR 214 28.834 67.062 64.683 1.00 20.61 DIC ATOM 1703 CE2 TYR 214 28.943 68.243 63.954 1.00 22.48 DIC ATOM 1704 CZ TYR 214 30.196 68.740 63.637 1.00 22.15 DIC ATOM 1705 OH TYR 214 30.304 69.912 62.914 1.00 23.53 DIC ATOM 1706 C TYR 214 29.045 66.363 67.939 1.00 16.93 DIC ATOM 1707 O TYR 214 29.375 67.506 68.254 1.00 16.76 DIC ATOM 1708 N ALA 215 27.792 65.929 68.011 1.00 18.68 DIC ATOM 1709 CA ALA 215 26.725 66.800 68.489 1.00 20.37 DIC ATOM 1710 CB ALA 215 25.399 66.039 68.505 1.00 20.09 DIC ATOM 1711 C ALA 215 27.064 67.326 69.888 1.00 22.19 DIC ATOM 1712 O ALA 215 26.742 68.465 70.229 1.00 22.00 DIC ATOM 1713 N ALA 216 27.734 66.501 70.686 1.00 23.55 DIC ATOM 1714 CA ALA 216 28.111 66.894 72.040 1.00 26.87 DIC ATOM 1715 CB ALA 216 28.597 65.676 72.822 1.00 26.18 DIC ATOM 1716 C ALA 216 29.176 67.995 72.060 1.00 29.18 DIC ATOM 1717 O ALA 216 29.416 68.606 73.097 1.00 29.39 DIC ATOM 1718 N MSE 217 29.814 68.244 70.919 1.00 31.87 DIC ATOM 1719 CA MSE 217 30.840 69.284 70.822 1.00 34.52 DIC ATOM 1720 CB MSE 217 31.525 69.245 69.453 1.00 37.00 DIC ATOM 1721 CG MSE 217 32.334 67.995 69.149 1.00 40.08 DIC ATOM 1722 SE MSE 217 33.910 67.778 70.249 1.00 46.50 DIC ATOM 1723 CE MSE 217 34.937 69.288 69.631 1.00 45.06 DIC ATOM 1724 C MSE 217 30.203 70.658 71.002 1.00 35.07 DIC ATOM 1725 OT1 MSE 217 30.688 71.459 71.837 1.00 15.87 DIC ATOM 1726 OT2 MSE 217 29.223 70.927 70.278 1.00 15.87 DIC ATOM 1727 CB PRO 222 24.458 67.558 78.759 1.00 28.83 DIC ATOM 1728 CG PRO 222 25.198 67.311 77.451 1.00 28.89 DIC ATOM 1729 C PRO 222 26.376 67.968 80.306 1.00 28.22 DIC ATOM 1730 O PRO 222 27.322 68.622 80.771 1.00 29.45 DIC ATOM 1731 N PRO 222 25.993 69.355 78.294 1.00 28.60 DIC ATOM 1732 CD PRO 222 25.675 68.707 77.009 1.00 29.20 DIC ATOM 1733 CA PRO 222 25.342 68.618 79.398 1.00 28.68 DIC ATOM 1734 N ALA 223 26.184 66.671 80.525 1.00 28.20 DIC ATOM 1735 CA ALA 223 27.038 65.838 81.366 1.00 27.95 DIC ATOM 1736 CB ALA 223 27.638 66.659 82.509 1.00 27.92 DIC ATOM 1737 C ALA 223 26.116 64.764 81.925 1.00 27.33 DIC ATOM 1738 O ALA 223 25.370 65.009 82.871 1.00 27.98 DIC ATOM 1739 N THR 224 26.158 63.578 81.335 1.00 27.53 DIC ATOM 1740 CA THR 224 25.294 62.494 81.787 1.00 27.74 DIC ATOM 1741 CB THR 224 25.194 61.402 80.692 1.00 27.45 DIC ATOM 1742 OG1 THR 224 25.090 60.106 81.294 1.00 28.28 DIC ATOM 1743 CG2 THR 224 26.408 61.470 79.761 1.00 29.04 DIC ATOM 1744 C THR 224 25.700 61.883 83.136 1.00 27.43 DIC ATOM 1745 O THR 224 24.856 61.344 83.856 1.00 28.04 DIC ATOM 1746 N HIS 225 26.981 61.983 83.480 1.00 26.82 DIC ATOM 1747 CA HIS 225 27.491 61.455 84.746 1.00 25.60 DIC ATOM 1748 CB HIS 225 28.100 60.070 84.541 1.00 25.60 DIC ATOM 1749 CG HIS 225 27.095 59.000 84.263 1.00 25.36 DIC ATOM 1750 CD2 HIS 225 26.818 58.309 83.132 1.00 24.64 DIC ATOM 1751 ND1 HIS 225 26.231 58.525 85.225 1.00 25.09 DIC ATOM 1752 CE1 HIS 225 25.466 57.585 84.700 1.00 24.96 DIC ATOM 1753 NE2 HIS 225 25.801 57.435 83.431 1.00 25.41 DIC ATOM 1754 C HIS 225 28.565 62.391 85.289 1.00 25.02 DIC ATOM 1755 O HIS 225 29.326 62.967 84.516 1.00 25.07 DIC ATOM 1756 N THR 226 28.634 62.535 86.613 1.00 24.57 DIC ATOM 1757 CA THR 226 29.633 63.410 87.231 1.00 23.66 DIC ATOM 1758 CB THR 226 29.152 63.957 88.600 1.00 23.68 DIC ATOM 1759 OG1 THR 226 28.822 62.867 89.470 1.00 23.32 DIC ATOM 1760 CG2 THR 226 27.930 64.841 88.419 1.00 24.26 DIC ATOM 1761 C THR 226 30.958 62.676 87.430 1.00 22.94 DIC ATOM 1762 O THR 226 32.015 63.300 87.558 1.00 22.50 DIC ATOM 1763 N ASP 227 30.889 61.348 87.454 1.00 22.21 DIC ATOM 1764 CA ASP 227 32.071 60.509 87.616 1.00 21.20 DIC ATOM 1765 CB ASP 227 31.749 59.079 87.179 1.00 22.48 DIC ATOM 1766 CG ASP 227 32.969 58.177 87.182 1.00 22.78 DIC ATOM 1767 OD1 ASP 227 32.906 57.089 86.574 1.00 23.40 DIC ATOM 1768 OD2 ASP 227 33.988 58.551 87.795 1.00 23.59 DIC ATOM 1769 C ASP 227 33.226 61.044 86.767 1.00 21.18 DIC ATOM 1770 O ASP 227 33.110 61.149 85.551 1.00 20.24 DIC ATOM 1771 N PRO 228 34.358 61.381 87.401 1.00 20.52 DIC ATOM 1772 CD PRO 228 34.630 61.341 88.848 1.00 20.97 DIC ATOM 1773 CA PRO 228 35.514 61.901 86.662 1.00 19.86 DIC ATOM 1774 CB PRO 228 36.526 62.205 87.768 1.00 21.04 DIC ATOM 1775 CG PRO 228 36.130 61.267 88.878 1.00 21.72 DIC ATOM 1776 C PRO 228 36.061 60.959 85.589 1.00 19.43 DIC ATOM 1777 O PRO 228 36.535 61.411 84.548 1.00 18.48 DIC ATOM 1778 N LEU 229 35.996 59.653 85.827 1.00 18.78 DIC ATOM 1779 CA LEU 229 36.489 58.703 84.832 1.00 18.33 DIC ATOM 1780 CB LEU 229 36.450 57.279 85.382 1.00 18.37 DIC ATOM 1781 CG LEU 229 36.958 56.164 84.464 1.00 19.20 DIC ATOM 1782 CD1 LEU 229 37.498 55.030 85.319 1.00 19.93 DIC ATOM 1783 CD2 LEU 229 35.842 55.677 83.540 1.00 19.78 DIC ATOM 1784 C LEU 229 35.618 58.800 83.588 1.00 17.34 DIC ATOM 1785 O LEU 229 36.119 58.932 82.467 1.00 17.32 DIC ATOM 1786 N TYR 230 34.308 58.742 83.802 1.00 17.15 DIC ATOM 1787 CA TYR 230 33.335 58.832 82.724 1.00 15.74 DIC ATOM 1788 CB TYR 230 31.919 58.923 83.292 1.00 16.08 DIC ATOM 1789 CG TYR 230 30.850 58.982 82.225 1.00 14.76 DIC ATOM 1790 CD1 TYR 230 30.422 57.827 81.580 1.00 14.83 DIC ATOM 1791 CE1 TYR 230 29.469 57.877 80.569 1.00 14.30 DIC ATOM 1792 CD2 TYR 230 30.296 60.199 81.835 1.00 14.34 DIC ATOM 1793 CE2 TYR 230 29.345 60.261 80.827 1.00 15.23 DIC ATOM 1794 CZ TYR 230 28.935 59.093 80.196 1.00 14.70 DIC ATOM 1795 OH TYR 230 27.993 59.146 79.190 1.00 14.53 DIC ATOM 1796 C TYR 230 33.601 60.075 81.892 1.00 16.16 DIC ATOM 1797 O TYR 230 33.603 60.027 80.665 1.00 15.11 DIC ATOM 1798 N ARG 231 33.809 61.195 82.574 1.00 16.82 DIC ATOM 1799 CA ARG 231 34.068 62.460 81.896 1.00 17.72 DIC ATOM 1800 CB ARG 231 34.045 63.606 82.915 1.00 20.64 DIC ATOM 1801 CG ARG 231 32.640 63.909 83.459 1.00 24.03 DIC ATOM 1802 CD ARG 231 32.702 64.690 84.769 1.00 27.73 DIC ATOM 1803 NE ARG 231 33.599 65.839 84.672 1.00 31.57 DIC ATOM 1804 CZ ARG 231 33.335 66.937 83.971 1.00 32.63 DIC ATOM 1805 NH1 ARG 231 34.216 67.930 83.933 1.00 33.24 DIC ATOM 1806 NH2 ARG 231 32.182 67.048 83.321 1.00 33.69 DIC ATOM 1807 C ARG 231 35.394 62.429 81.143 1.00 17.46 DIC ATOM 1808 O ARG 231 35.499 62.956 80.036 1.00 16.04 DIC ATOM 1809 N ASP 232 36.402 61.798 81.736 1.00 16.62 DIC ATOM 1810 CA ASP 232 37.708 61.710 81.097 1.00 17.02 DIC ATOM 1811 CB ASP 232 38.698 61.039 82.055 1.00 16.63 DIC ATOM 1812 CG ASP 232 40.058 60.792 81.425 1.00 18.06 DIC ATOM 1813 OD1 ASP 232 40.216 59.786 80.698 1.00 18.50 DIC ATOM 1814 OD2 ASP 232 40.976 61.602 81.662 1.00 17.41 DIC ATOM 1815 C ASP 232 37.625 60.939 79.771 1.00 16.91 DIC ATOM 1816 O ASP 232 38.189 61.362 78.755 1.00 16.81 DIC ATOM 1817 N ARG 233 36.897 59.825 79.781 1.00 16.06 DIC ATOM 1818 CA ARG 233 36.748 58.985 78.598 1.00 14.55 DIC ATOM 1819 CB ARG 233 36.210 57.605 78.993 1.00 14.82 DIC ATOM 1820 CG ARG 233 37.033 56.881 80.036 1.00 13.79 DIC ATOM 1821 CD ARG 233 38.393 56.443 79.515 1.00 13.23 DIC ATOM 1822 NE ARG 233 39.008 55.517 80.460 1.00 13.51 DIC ATOM 1823 CZ ARG 233 39.560 55.875 81.618 1.00 14.87 DIC ATOM 1824 NH1 ARG 233 39.596 57.151 81.982 1.00 13.99 DIC ATOM 1825 NH2 ARG 233 40.042 54.947 82.435 1.00 13.15 DIC ATOM 1826 C ARG 233 35.830 59.572 77.533 1.00 14.38 DIC ATOM 1827 O ARG 233 36.076 59.396 76.341 1.00 14.52 DIC ATOM 1828 N THR 234 34.774 60.262 77.955 1.00 13.26 DIC ATOM 1829 CA THR 234 33.830 60.831 77.000 1.00 12.89 DIC ATOM 1830 CB THR 234 32.419 60.981 77.622 1.00 11.52 DIC ATOM 1831 OG1 THR 234 32.512 61.637 78.893 1.00 9.01 DIC ATOM 1832 CG2 THR 234 31.782 59.605 77.807 1.00 10.76 DIC ATOM 1833 C THR 234 34.283 62.153 76.399 1.00 13.61 DIC ATOM 1834 O THR 234 33.754 62.577 75.384 1.00 13.22 DIC ATOM 1835 N ASN 235 35.258 62.802 77.028 1.00 14.53 DIC ATOM 1836 CA ASN 235 35.802 64.048 76.501 1.00 15.83 DIC ATOM 1837 CB ASN 235 36.519 64.854 77.590 1.00 18.71 DIC ATOM 1838 CG ASN 235 37.384 65.976 77.009 1.00 20.95 DIC ATOM 1839 OD1 ASN 235 36.880 67.030 76.616 1.00 22.71 DIC ATOM 1840 ND2 ASN 235 38.693 65.739 76.935 1.00 23.01 DIC ATOM 1841 C ASN 235 36.822 63.618 75.457 1.00 15.52 DIC ATOM 1842 O ASN 235 37.901 63.125 75.794 1.00 13.95 DIC ATOM 1843 N THR 236 36.485 63.795 74.188 1.00 14.36 DIC ATOM 1844 CA THR 236 37.396 63.397 73.135 1.00 14.17 DIC ATOM 1845 CB THR 236 36.711 63.494 71.754 1.00 14.16 DIC ATOM 1846 OG1 THR 236 35.656 62.523 71.690 1.00 12.60 DIC ATOM 1847 CG2 THR 236 37.716 63.234 70.622 1.00 13.57 DIC ATOM 1848 C THR 236 38.667 64.228 73.142 1.00 14.15 DIC ATOM 1849 O THR 236 38.619 65.460 73.213 1.00 15.30 DIC ATOM 1850 N VAL 237 39.808 63.546 73.105 1.00 13.96 DIC ATOM 1851 CA VAL 237 41.094 64.227 73.070 1.00 14.29 DIC ATOM 1852 CB VAL 237 42.190 63.454 73.866 1.00 14.32 DIC ATOM 1853 CG1 VAL 237 43.530 64.173 73.749 1.00 14.22 DIC ATOM 1854 CG2 VAL 237 41.794 63.349 75.335 1.00 13.45 DIC ATOM 1855 C VAL 237 41.471 64.268 71.594 1.00 14.08 DIC ATOM 1856 O VAL 237 41.763 63.231 70.996 1.00 13.74 DIC ATOM 1857 N MSE 238 41.423 65.461 71.004 1.00 14.13 DIC ATOM 1858 CA MSE 238 41.753 65.636 69.593 1.00 14.57 DIC ATOM 1859 CB MSE 238 41.525 67.095 69.170 1.00 15.84 DIC ATOM 1860 CG MSE 238 40.078 67.574 69.271 1.00 18.43 DIC ATOM 1861 SE MSE 238 38.879 66.542 68.173 1.00 23.28 DIC ATOM 1862 CE MSE 238 37.208 66.992 69.030 1.00 22.22 DIC ATOM 1863 C MSE 238 43.205 65.251 69.313 1.00 13.92 DIC ATOM 1864 O MSE 238 44.050 65.297 70.208 1.00 13.64 DIC ATOM 1865 N PRO 239 43.508 64.845 68.066 1.00 13.35 DIC ATOM 1866 CD PRO 239 44.889 64.645 67.591 1.00 14.11 DIC ATOM 1867 CA PRO 239 42.566 64.743 66.949 1.00 13.23 DIC ATOM 1868 CB PRO 239 43.477 64.777 65.728 1.00 14.00 DIC ATOM 1869 CG PRO 239 44.675 64.036 66.220 1.00 14.44 DIC ATOM 1870 C PRO 239 41.761 63.452 67.009 1.00 13.04 DIC ATOM 1871 O PRO 239 42.125 62.512 67.721 1.00 12.63 DIC ATOM 1872 N VAL 240 40.668 63.417 66.253 1.00 12.39 DIC ATOM 1873 CA VAL 240 39.824 62.240 66.199 1.00 11.18 DIC ATOM 1874 CB VAL 240 38.567 62.506 65.352 1.00 11.67 DIC ATOM 1875 CG1 VAL 240 37.728 61.238 65.244 1.00 11.57 DIC ATOM 1876 CG2 VAL 240 37.755 63.641 65.980 1.00 11.98 DIC ATOM 1877 C VAL 240 40.660 61.150 65.550 1.00 10.08 DIC ATOM 1878 O VAL 240 41.329 61.403 64.553 1.00 9.26 DIC ATOM 1879 N ALA 241 40.645 59.951 66.125 1.00 8.61 DIC ATOM 1880 CA ALA 241 41.423 58.834 65.582 1.00 8.11 DIC ATOM 1881 CB ALA 241 42.072 58.040 66.716 1.00 8.10 DIC ATOM 1882 C ALA 241 40.545 57.916 64.739 1.00 7.76 DIC ATOM 1883 O ALA 241 41.000 57.341 63.749 1.00 7.78 DIC ATOM 1884 N VAL 242 39.282 57.788 65.133 1.00 7.63 DIC ATOM 1885 CA VAL 242 38.334 56.948 64.410 1.00 7.88 DIC ATOM 1886 CB VAL 242 38.101 55.605 65.152 1.00 6.91 DIC ATOM 1887 CG1 VAL 242 37.159 54.716 64.334 1.00 7.05 DIC ATOM 1888 CG2 VAL 242 39.435 54.894 65.400 1.00 5.82 DIC ATOM 1889 C VAL 242 36.965 57.599 64.228 1.00 9.17 DIC ATOM 1890 O VAL 242 36.296 57.908 65.207 1.00 9.42 DIC ATOM 1891 N SER 243 36.560 57.818 62.979 1.00 10.01 DIC ATOM 1892 CA SER 243 35.235 58.359 62.692 1.00 10.35 DIC ATOM 1893 CB SER 243 35.219 59.157 61.379 1.00 11.55 DIC ATOM 1894 OG SER 243 35.705 60.470 61.551 1.00 13.46 DIC ATOM 1895 C SER 243 34.356 57.133 62.530 1.00 10.90 DIC ATOM 1896 O SER 243 34.697 56.221 61.774 1.00 12.28 DIC ATOM 1897 N HIS 244 33.248 57.087 63.260 1.00 10.40 DIC ATOM 1898 CA HIS 244 32.335 55.955 63.157 1.00 9.48 DIC ATOM 1899 CB HIS 244 32.258 55.211 64.491 1.00 8.63 DIC ATOM 1900 CG HIS 244 31.406 53.969 64.457 1.00 7.07 DIC ATOM 1901 CD2 HIS 244 30.800 53.324 63.430 1.00 6.40 DIC ATOM 1902 ND1 HIS 244 31.109 53.242 65.593 1.00 5.32 DIC ATOM 1903 CE1 HIS 244 30.358 52.203 65.268 1.00 6.23 DIC ATOM 1904 NE2 HIS 244 30.155 52.228 63.961 1.00 5.08 DIC ATOM 1905 C HIS 244 30.962 56.518 62.778 1.00 9.32 DIC ATOM 1906 O HIS 244 30.357 57.262 63.518 1.00 9.29 DIC ATOM 1907 N TYR 245 30.491 56.106 61.614 1.00 10.23 DIC ATOM 1908 CA TYR 245 29.229 56.554 61.093 1.00 11.52 DIC ATOM 1909 CB TYR 245 29.385 56.723 59.580 1.00 12.42 DIC ATOM 1910 CG TYR 245 30.457 57.727 59.231 1.00 13.35 DIC ATOM 1911 CD1 TYR 245 30.201 59.088 59.354 1.00 14.28 DIC ATOM 1912 CE1 TYR 245 31.183 60.030 59.167 1.00 14.76 DIC ATOM 1913 CD2 TYR 245 31.750 57.323 58.888 1.00 13.50 DIC ATOM 1914 CE2 TYR 245 32.760 58.273 58.692 1.00 14.51 DIC ATOM 1915 CZ TYR 245 32.455 59.626 58.845 1.00 14.66 DIC ATOM 1916 OH TYR 245 33.392 60.623 58.735 1.00 16.02 DIC ATOM 1917 C TYR 245 28.023 55.657 61.442 1.00 12.60 DIC ATOM 1918 O TYR 245 27.217 55.324 60.565 1.00 10.16 DIC ATOM 1919 N CYS 246 27.868 55.278 62.716 1.00 14.89 DIC ATOM 1920 CA CYS 246 26.747 54.389 63.105 1.00 14.89 DIC ATOM 1921 CB CYS 246 26.837 54.053 64.586 1.00 14.89 DIC ATOM 1922 SG CYS 246 26.840 55.482 65.652 1.00 14.89 DIC ATOM 1923 C CYS 246 25.358 54.973 62.774 1.00 14.89 DIC ATOM 1924 O CYS 246 25.166 56.192 62.672 1.00 17.31 DIC ATOM 1925 N GLY 247 24.386 54.085 62.600 1.00 17.22 DIC ATOM 1926 CA GLY 247 23.050 54.509 62.224 1.00 15.49 DIC ATOM 1927 C GLY 247 22.836 54.344 60.719 1.00 15.79 DIC ATOM 1928 O GLY 247 23.737 53.891 60.024 1.00 14.94 DIC ATOM 1929 N PRO 248 21.638 54.668 60.197 1.00 15.38 DIC ATOM 1930 CD PRO 248 20.497 55.170 60.986 1.00 15.79 DIC ATOM 1931 CA PRO 248 21.275 54.566 58.776 1.00 15.64 DIC ATOM 1932 CB PRO 248 19.790 54.933 58.781 1.00 16.59 DIC ATOM 1933 CG PRO 248 19.691 55.890 59.926 1.00 16.76 DIC ATOM 1934 C PRO 248 22.078 55.449 57.812 1.00 15.27 DIC ATOM 1935 O PRO 248 22.254 55.102 56.643 1.00 14.87 DIC ATOM 1936 N ALA 249 22.558 56.590 58.301 1.00 15.42 DIC ATOM 1937 CA ALA 249 23.315 57.528 57.468 1.00 15.19 DIC ATOM 1938 CB ALA 249 23.165 58.938 58.029 1.00 15.27 DIC ATOM 1939 C ALA 249 24.793 57.173 57.328 1.00 15.38 DIC ATOM 1940 O ALA 249 25.592 57.446 58.220 1.00 15.05 DIC ATOM 1941 N LYS 250 25.152 56.584 56.188 1.00 14.72 DIC ATOM 1942 CA LYS 250 26.531 56.180 55.938 1.00 15.73 DIC ATOM 1943 CB LYS 250 26.566 54.754 55.382 1.00 13.72 DIC ATOM 1944 CG LYS 250 25.816 53.722 56.234 1.00 12.46 DIC ATOM 1945 CD LYS 250 26.365 53.637 57.655 1.00 11.65 DIC ATOM 1946 CE LYS 250 25.760 52.454 58.410 1.00 10.42 DIC ATOM 1947 NZ LYS 250 26.120 52.501 59.856 1.00 8.32 DIC ATOM 1948 C LYS 250 27.238 57.129 54.968 1.00 16.91 DIC ATOM 1949 O LYS 250 26.590 57.809 54.180 1.00 17.59 DIC ATOM 1950 N PRO 251 28.582 57.170 55.006 1.00 18.44 DIC ATOM 1951 CD PRO 251 29.488 56.380 55.861 1.00 18.27 DIC ATOM 1952 CA PRO 251 29.348 58.049 54.118 1.00 19.06 DIC ATOM 1953 CB PRO 251 30.767 57.936 54.663 1.00 18.51 DIC ATOM 1954 CG PRO 251 30.820 56.527 55.144 1.00 19.13 DIC ATOM 1955 C PRO 251 29.261 57.682 52.641 1.00 20.28 DIC ATOM 1956 O PRO 251 29.504 58.531 51.781 1.00 20.27 DIC ATOM 1957 N TRP 252 28.919 56.429 52.341 1.00 20.96 DIC ATOM 1958 CA TRP 252 28.799 55.997 50.945 1.00 21.97 DIC ATOM 1959 CB TRP 252 29.103 54.497 50.803 1.00 19.99 DIC ATOM 1960 CG TRP 252 28.408 53.601 51.785 1.00 17.82 DIC ATOM 1961 CD2 TRP 252 28.983 53.017 52.960 1.00 17.40 DIC ATOM 1962 CE2 TRP 252 27.976 52.253 53.581 1.00 16.50 DIC ATOM 1963 CE3 TRP 252 30.254 53.069 53.548 1.00 15.92 DIC ATOM 1964 CD1 TRP 252 27.113 53.180 51.743 1.00 17.54 DIC ATOM 1965 NE1 TRP 252 26.846 52.370 52.819 1.00 16.77 DIC ATOM 1966 CZ2 TRP 252 28.198 51.545 54.760 1.00 16.16 DIC ATOM 1967 CZ3 TRP 252 30.474 52.363 54.723 1.00 15.63 DIC ATOM 1968 CH2 TRP 252 29.451 51.612 55.316 1.00 16.00 DIC ATOM 1969 C TRP 252 27.420 56.320 50.375 1.00 23.39 DIC ATOM 1970 O TRP 252 27.060 55.873 49.284 1.00 23.70 DIC ATOM 1971 N HIS 253 26.666 57.117 51.125 1.00 25.29 DIC ATOM 1972 CA HIS 253 25.328 57.546 50.735 1.00 27.91 DIC ATOM 1973 CB HIS 253 24.389 57.480 51.941 1.00 28.69 DIC ATOM 1974 CG HIS 253 23.900 56.102 52.247 1.00 29.56 DIC ATOM 1975 CD2 HIS 253 23.892 54.973 51.499 1.00 29.18 DIC ATOM 1976 ND1 HIS 253 23.314 55.769 53.451 1.00 29.91 DIC ATOM 1977 CE1 HIS 253 22.969 54.494 53.431 1.00 30.98 DIC ATOM 1978 NE2 HIS 253 23.310 53.988 52.258 1.00 30.37 DIC ATOM 1979 C HIS 253 25.353 58.972 50.187 1.00 28.54 DIC ATOM 1980 OT1 HIS 253 26.453 59.565 50.159 1.00 15.87 DIC ATOM 1981 OT2 HIS 253 24.275 59.480 49.790 1.00 15.87 DIC ATOM 1982 CB ALA 258 28.094 61.904 58.825 1.00 28.44 DIC ATOM 1983 C ALA 258 29.433 64.012 58.929 1.00 27.58 DIC ATOM 1984 O ALA 258 29.918 64.149 57.808 1.00 27.40 DIC ATOM 1985 N ALA 258 27.094 64.069 58.174 1.00 28.06 DIC ATOM 1986 CA ALA 258 28.048 63.405 59.105 1.00 27.73 DIC ATOM 1987 N TRP 259 30.068 64.366 60.042 1.00 27.44 DIC ATOM 1988 CA TRP 259 31.396 64.976 60.013 1.00 26.88 DIC ATOM 1989 CB TRP 259 31.824 65.387 61.426 1.00 27.00 DIC ATOM 1990 CG TRP 259 33.185 66.030 61.464 1.00 26.63 DIC ATOM 1991 CD2 TRP 259 34.417 65.401 61.831 1.00 26.39 DIC ATOM 1992 CE2 TRP 259 35.440 66.363 61.676 1.00 26.47 DIC ATOM 1993 CE3 TRP 259 34.758 64.117 62.276 1.00 26.52 DIC ATOM 1994 CD1 TRP 259 33.499 67.312 61.111 1.00 26.17 DIC ATOM 1995 NE1 TRP 259 34.853 67.520 61.236 1.00 26.25 DIC ATOM 1996 CZ2 TRP 259 36.779 66.080 61.948 1.00 26.25 DIC ATOM 1997 CZ3 TRP 259 36.090 63.837 62.546 1.00 25.96 DIC ATOM 1998 CH2 TRP 259 37.083 64.815 62.381 1.00 26.60 DIC ATOM 1999 C TRP 259 32.465 64.060 59.419 1.00 26.25 DIC ATOM 2000 O TRP 259 32.511 62.869 59.723 1.00 26.62 DIC ATOM 2001 N GLY 260 33.314 64.632 58.570 1.00 25.54 DIC ATOM 2002 CA GLY 260 34.400 63.889 57.949 1.00 24.64 DIC ATOM 2003 C GLY 260 34.002 62.871 56.898 1.00 24.46 DIC ATOM 2004 O GLY 260 34.833 62.072 56.462 1.00 25.49 DIC ATOM 2005 N ALA 261 32.742 62.899 56.479 1.00 24.06 DIC ATOM 2006 CA ALA 261 32.247 61.958 55.484 1.00 23.45 DIC ATOM 2007 CB ALA 261 30.744 62.142 55.310 1.00 23.85 DIC ATOM 2008 C ALA 261 32.946 62.072 54.131 1.00 23.44 DIC ATOM 2009 O ALA 261 32.868 61.161 53.315 1.00 24.03 DIC ATOM 2010 N ALA 262 33.631 63.185 53.889 1.00 23.25 DIC ATOM 2011 CA ALA 262 34.318 63.387 52.615 1.00 23.00 DIC ATOM 2012 CB ALA 262 34.643 64.869 52.415 1.00 23.30 DIC ATOM 2013 C ALA 262 35.589 62.560 52.484 1.00 22.59 DIC ATOM 2014 O ALA 262 36.061 62.312 51.374 1.00 22.28 DIC ATOM 2015 N ARG 263 36.159 62.144 53.607 1.00 21.93 DIC ATOM 2016 CA ARG 263 37.370 61.347 53.550 1.00 21.92 DIC ATOM 2017 CB ARG 263 37.959 61.155 54.950 1.00 24.12 DIC ATOM 2018 CG ARG 263 39.231 60.298 54.987 1.00 27.56 DIC ATOM 2019 CD ARG 263 39.921 60.412 56.350 1.00 30.65 DIC ATOM 2020 NE ARG 263 40.887 59.343 56.622 1.00 33.18 DIC ATOM 2021 CZ ARG 263 41.943 59.055 55.862 1.00 34.55 DIC ATOM 2022 NH1 ARG 263 42.757 58.064 56.210 1.00 35.10 DIC ATOM 2023 NH2 ARG 263 42.183 59.748 54.751 1.00 35.66 DIC ATOM 2024 C ARG 263 37.062 59.998 52.906 1.00 20.84 DIC ATOM 2025 O ARG 263 37.951 59.357 52.359 1.00 19.59 DIC ATOM 2026 N PHE 264 35.803 59.569 52.971 1.00 20.19 DIC ATOM 2027 CA PHE 264 35.403 58.300 52.360 1.00 19.21 DIC ATOM 2028 CB PHE 264 33.941 57.972 52.676 1.00 19.33 DIC ATOM 2029 CG PHE 264 33.437 56.740 51.971 1.00 18.65 DIC ATOM 2030 CD1 PHE 264 33.600 55.480 52.536 1.00 17.83 DIC ATOM 2031 CD2 PHE 264 32.844 56.835 50.712 1.00 17.86 DIC ATOM 2032 CE1 PHE 264 33.182 54.329 51.857 1.00 17.13 DIC ATOM 2033 CE2 PHE 264 32.427 55.694 50.031 1.00 18.25 DIC ATOM 2034 CZ PHE 264 32.596 54.440 50.604 1.00 16.55 DIC ATOM 2035 C PHE 264 35.560 58.371 50.844 1.00 19.58 DIC ATOM 2036 O PHE 264 36.246 57.545 50.235 1.00 18.31 DIC ATOM 2037 N THR 265 34.909 59.357 50.233 1.00 20.22 DIC ATOM 2038 CA THR 265 34.976 59.523 48.783 1.00 21.42 DIC ATOM 2039 CB THR 265 34.038 60.674 48.309 1.00 22.32 DIC ATOM 2040 OG1 THR 265 34.270 60.945 46.920 1.00 23.37 DIC ATOM 2041 CG2 THR 265 34.268 61.927 49.111 1.00 23.03 DIC ATOM 2042 C THR 265 36.419 59.780 48.342 1.00 21.65 DIC ATOM 2043 O THR 265 36.855 59.319 47.287 1.00 20.87 DIC ATOM 2044 N GLU 266 37.167 60.485 49.180 1.00 21.89 DIC ATOM 2045 CA GLU 266 38.560 60.794 48.899 1.00 22.68 DIC ATOM 2046 CB GLU 266 39.086 61.722 49.989 1.00 24.83 DIC ATOM 2047 CG GLU 266 40.501 62.213 49.792 1.00 29.43 DIC ATOM 2048 CD GLU 266 40.812 63.387 50.704 1.00 31.88 DIC ATOM 2049 OE1 GLU 266 40.454 63.314 51.903 1.00 32.56 DIC ATOM 2050 OE2 GLU 266 41.410 64.380 50.223 1.00 33.53 DIC ATOM 2051 C GLU 266 39.394 59.504 48.824 1.00 21.84 DIC ATOM 2052 O GLU 266 40.229 59.348 47.935 1.00 20.75 DIC ATOM 2053 N LEU 267 39.162 58.584 49.760 1.00 19.85 DIC ATOM 2054 CA LEU 267 39.874 57.308 49.780 1.00 19.01 DIC ATOM 2055 CB LEU 267 39.643 56.581 51.105 1.00 18.80 DIC ATOM 2056 CG LEU 267 40.471 57.095 52.276 1.00 18.91 DIC ATOM 2057 CD1 LEU 267 39.894 56.591 53.588 1.00 18.99 DIC ATOM 2058 CD2 LEU 267 41.914 56.654 52.082 1.00 19.67 DIC ATOM 2059 C LEU 267 39.406 56.425 48.639 1.00 18.45 DIC ATOM 2060 O LEU 267 40.215 55.764 47.992 1.00 16.88 DIC ATOM 2061 N ALA 268 38.095 56.408 48.398 1.00 18.86 DIC ATOM 2062 CA ALA 268 37.532 55.607 47.318 1.00 20.48 DIC ATOM 2063 CB ALA 268 36.018 55.792 47.254 1.00 21.06 DIC ATOM 2064 C ALA 268 38.169 56.024 45.996 1.00 21.58 DIC ATOM 2065 O ALA 268 38.481 55.185 45.157 1.00 20.74 DIC ATOM 2066 N GLY 269 38.376 57.324 45.820 1.00 22.51 DIC ATOM 2067 CA GLY 269 38.979 57.805 44.590 1.00 24.41 DIC ATOM 2068 C GLY 269 40.444 57.429 44.473 1.00 25.41 DIC ATOM 2069 O GLY 269 41.007 57.421 43.379 1.00 25.74 DIC ATOM 2070 N SER 270 41.069 57.114 45.600 1.00 25.49 DIC ATOM 2071 CA SER 270 42.479 56.748 45.598 1.00 26.14 DIC ATOM 2072 CB SER 270 43.117 57.107 46.939 1.00 25.67 DIC ATOM 2073 OG SER 270 42.648 56.249 47.965 1.00 25.26 DIC ATOM 2074 C SER 270 42.689 55.263 45.329 1.00 26.42 DIC ATOM 2075 O SER 270 43.821 54.815 45.155 1.00 26.83 DIC ATOM 2076 N LEU 271 41.603 54.498 45.298 1.00 26.90 DIC ATOM 2077 CA LEU 271 41.708 53.063 45.065 1.00 27.83 DIC ATOM 2078 CB LEU 271 40.319 52.417 45.034 1.00 27.48 DIC ATOM 2079 CG LEU 271 39.575 52.392 46.367 1.00 27.23 DIC ATOM 2080 CD1 LEU 271 38.288 51.595 46.216 1.00 26.49 DIC ATOM 2081 CD2 LEU 271 40.470 51.778 47.435 1.00 26.56 DIC ATOM 2082 C LEU 271 42.460 52.696 43.793 1.00 28.34 DIC ATOM 2083 O LEU 271 42.286 53.314 42.744 1.00 28.17 DIC ATOM 2084 N THR 272 43.289 51.665 43.907 1.00 29.25 DIC ATOM 2085 CA THR 272 44.088 51.166 42.799 1.00 29.35 DIC ATOM 2086 CB THR 272 45.106 50.129 43.293 1.00 29.61 DIC ATOM 2087 OG1 THR 272 45.930 50.712 44.312 1.00 30.29 DIC ATOM 2088 CG2 THR 272 45.974 49.654 42.142 1.00 29.87 DIC ATOM 2089 C THR 272 43.229 50.500 41.728 1.00 29.37 DIC ATOM 2090 O THR 272 43.324 50.838 40.548 1.00 29.51 DIC ATOM 2091 N THR 273 42.409 49.541 42.151 1.00 28.69 DIC ATOM 2092 CA THR 273 41.533 48.798 41.248 1.00 28.59 DIC ATOM 2093 CB THR 273 41.892 47.297 41.218 1.00 30.32 DIC ATOM 2094 OG1 THR 273 43.302 47.137 41.014 1.00 32.39 DIC ATOM 2095 CG2 THR 273 41.140 46.602 40.096 1.00 31.41 DIC ATOM 2096 C THR 273 40.077 48.896 41.690 1.00 27.15 DIC ATOM 2097 O THR 273 39.746 48.572 42.831 1.00 26.61 DIC ATOM 2098 N VAL 274 39.204 49.334 40.789 1.00 24.82 DIC ATOM 2099 CA VAL 274 37.792 49.445 41.128 1.00 23.71 DIC ATOM 2100 CB VAL 274 37.361 50.924 41.261 1.00 24.47 DIC ATOM 2101 CG1 VAL 274 37.742 51.692 40.014 1.00 24.70 DIC ATOM 2102 CG2 VAL 274 35.862 51.005 41.509 1.00 24.49 DIC ATOM 2103 C VAL 274 36.917 48.739 40.095 1.00 22.44 DIC ATOM 2104 O VAL 274 36.769 49.202 38.964 1.00 21.71 DIC ATOM 2105 N PRO 275 36.341 47.587 40.477 1.00 21.18 DIC ATOM 2106 CD PRO 275 36.537 46.929 41.779 1.00 20.08 DIC ATOM 2107 CA PRO 275 35.472 46.778 39.619 1.00 20.90 DIC ATOM 2108 CB PRO 275 35.053 45.630 40.534 1.00 20.65 DIC ATOM 2109 CG PRO 275 36.203 45.498 41.464 1.00 20.01 DIC ATOM 2110 C PRO 275 34.267 47.558 39.120 1.00 20.92 DIC ATOM 2111 O PRO 275 33.714 48.397 39.835 1.00 20.31 DIC ATOM 2112 N GLU 276 33.859 47.273 37.890 1.00 22.03 DIC ATOM 2113 CA GLU 276 32.701 47.938 37.312 1.00 22.81 DIC ATOM 2114 CB GLU 276 32.317 47.269 35.987 1.00 23.16 DIC ATOM 2115 CG GLU 276 30.944 47.665 35.449 1.00 23.75 DIC ATOM 2116 CD GLU 276 30.859 49.123 35.047 1.00 23.43 DIC ATOM 2117 OE1 GLU 276 31.868 49.846 35.176 1.00 24.18 DIC ATOM 2118 OE2 GLU 276 29.774 49.547 34.598 1.00 24.32 DIC ATOM 2119 C GLU 276 31.540 47.843 38.293 1.00 23.40 DIC ATOM 2120 O GLU 276 30.810 48.811 38.496 1.00 24.06 DIC ATOM 2121 N GLU 277 31.395 46.683 38.928 1.00 23.55 DIC ATOM 2122 CA GLU 277 30.303 46.472 39.865 1.00 24.83 DIC ATOM 2123 CB GLU 277 30.148 44.976 40.157 1.00 27.38 DIC ATOM 2124 CG GLU 277 28.685 44.509 40.248 1.00 31.14 DIC ATOM 2125 CD GLU 277 28.029 44.257 38.882 1.00 33.24 DIC ATOM 2126 OE1 GLU 277 28.023 45.164 38.017 1.00 34.02 DIC ATOM 2127 OE2 GLU 277 27.508 43.136 38.679 1.00 34.95 DIC ATOM 2128 C GLU 277 30.419 47.255 41.180 1.00 23.83 DIC ATOM 2129 O GLU 277 29.507 47.209 42.009 1.00 24.63 DIC ATOM 2130 N TRP 278 31.532 47.964 41.373 1.00 22.09 DIC ATOM 2131 CA TRP 278 31.735 48.775 42.580 1.00 20.45 DIC ATOM 2132 CB TRP 278 33.183 48.680 43.078 1.00 17.96 DIC ATOM 2133 CG TRP 278 33.544 47.431 43.835 1.00 16.02 DIC ATOM 2134 CD2 TRP 278 34.693 47.245 44.677 1.00 16.17 DIC ATOM 2135 CE2 TRP 278 34.676 45.906 45.117 1.00 16.04 DIC ATOM 2136 CE3 TRP 278 35.738 48.084 45.101 1.00 16.30 DIC ATOM 2137 CD1 TRP 278 32.897 46.235 43.804 1.00 15.72 DIC ATOM 2138 NE1 TRP 278 33.569 45.312 44.568 1.00 15.84 DIC ATOM 2139 CZ2 TRP 278 35.665 45.378 45.959 1.00 15.03 DIC ATOM 2140 CZ3 TRP 278 36.728 47.557 45.941 1.00 15.75 DIC ATOM 2141 CH2 TRP 278 36.679 46.216 46.360 1.00 16.12 DIC ATOM 2142 C TRP 278 31.453 50.236 42.248 1.00 20.70 DIC ATOM 2143 O TRP 278 31.281 51.066 43.141 1.00 20.71 DIC ATOM 2144 N ALA 279 31.416 50.542 40.955 1.00 21.39 DIC ATOM 2145 CA ALA 279 31.190 51.904 40.479 1.00 22.71 DIC ATOM 2146 CB ALA 279 31.084 51.910 38.954 1.00 23.51 DIC ATOM 2147 C ALA 279 29.965 52.563 41.087 1.00 23.55 DIC ATOM 2148 O ALA 279 29.959 53.771 41.323 1.00 24.28 DIC ATOM 2149 N GLY 280 28.929 51.768 41.333 1.00 24.37 DIC ATOM 2150 CA GLY 280 27.705 52.294 41.913 1.00 25.98 DIC ATOM 2151 C GLY 280 27.849 52.651 43.383 1.00 26.65 DIC ATOM 2152 O GLY 280 27.674 53.808 43.770 1.00 27.02 DIC ATOM 2153 N ALA 281 28.165 51.657 44.208 1.00 27.42 DIC ATOM 2154 CA ALA 281 28.337 51.874 45.639 1.00 28.02 DIC ATOM 2155 CB ALA 281 28.645 50.550 46.334 1.00 27.29 DIC ATOM 2156 C ALA 281 29.477 52.860 45.857 1.00 28.66 DIC ATOM 2157 O ALA 281 29.529 53.550 46.874 1.00 29.25 DIC ATOM 2158 N ALA 282 30.377 52.912 44.879 1.00 29.42 DIC ATOM 2159 CA ALA 282 31.552 53.784 44.887 1.00 30.55 DIC ATOM 2160 CB ALA 282 31.121 55.261 44.884 1.00 30.21 DIC ATOM 2161 C ALA 282 32.458 53.501 46.078 1.00 31.20 DIC ATOM 2162 OT1 ALA 282 33.390 52.669 45.938 1.00 32.04 DIC ATOM 2163 OT2 ALA 282 32.207 54.100 47.145 1.00 31.25 DIC ATOM 2164 N1 UPG 341 27.240 44.499 57.825 1.00 10.18 ATOM 2165 C2 UPG 341 27.623 43.818 56.650 1.00 9.69 ATOM 2166 N3 UPG 341 26.746 44.059 55.575 1.00 8.84 ATOM 2167 C4 UPG 341 25.566 44.894 55.582 1.00 8.96 ATOM 2168 C5 UPG 341 25.252 45.558 56.815 1.00 8.24 ATOM 2169 C6 UPG 341 26.056 45.357 57.869 1.00 8.97 ATOM 2170 O2 UPG 341 28.602 43.097 56.579 1.00 9.27 ATOM 2171 O4 UPG 341 24.905 44.993 54.563 1.00 11.09 ATOM 2172 C4* UPG 341 28.140 45.874 61.110 1.00 9.66 ATOM 2173 O4* UPG 341 27.321 44.837 60.426 1.00 9.94 ATOM 2174 C3* UPG 341 28.902 46.508 59.951 1.00 8.28 ATOM 2175 O3* UPG 341 29.996 47.267 60.429 1.00 10.54 ATOM 2176 C2* UPG 341 29.173 45.283 59.098 1.00 9.24 ATOM 2177 O2* UPG 341 30.290 44.505 59.538 1.00 9.22 ATOM 2178 C1* UPG 341 27.913 44.478 59.203 1.00 10.37 ATOM 2179 C5* UPG 341 26.834 46.274 61.715 1.00 8.33 ATOM 2180 O5* UPG 341 26.278 47.636 61.455 1.00 14.17 ATOM 2181 PA UPG 341 26.757 49.151 61.231 1.00 11.35 ATOM 2182 O1A UPG 341 28.224 49.345 61.258 1.00 12.96 ATOM 2183 O2A UPG 341 26.106 49.722 60.020 1.00 14.14 ATOM 2184 O3A UPG 341 25.990 49.305 62.626 1.00 12.31 ATOM 2185 PB UPG 341 25.718 50.499 63.635 1.00 14.51 ATOM 2186 O1B UPG 341 27.055 51.134 63.729 1.00 11.54 ATOM 2187 O2B UPG 341 24.736 51.411 63.036 1.00 15.63 ATOM 2188 O3B UPG 341 25.289 49.955 65.021 1.00 15.47 ATOM 2189 C1′ UPG 341 25.701 49.765 66.543 1.00 20.67 ATOM 2190 C2′ UPG 341 27.182 49.323 66.490 1.00 19.41 ATOM 2191 C3′ UPG 341 27.600 48.129 65.515 1.00 20.26 ATOM 2192 C4′ UPG 341 26.609 46.923 65.726 1.00 19.77 ATOM 2193 C5′ UPG 341 25.121 47.545 65.719 1.00 20.08 ATOM 2194 C6′ UPG 341 24.111 46.486 66.179 1.00 21.34 ATOM 2195 F2′ UPG 341 28.054 50.401 66.263 1.00 22.29 ATOM 2196 O3′ UPG 341 28.884 47.722 65.901 1.00 19.02 ATOM 2197 O4′ UPG 341 26.927 46.281 66.991 1.00 18.02 ATOM 2198 O5′ UPG 341 24.861 48.621 66.750 1.00 20.07 ATOM 2199 O6′ UPG 341 23.853 45.237 65.594 1.00 20.34 ATOM 2200 MN MN 400 29.038 50.750 62.751 1.00 6.12 MN ATOM 2201 C1 LAT 1347 21.862 53.689 65.707 1.00 20.18 ATOM 2202 C2 LAT 1347 22.118 52.340 65.066 1.00 20.18 ATOM 2203 C3 LAT 1347 22.177 51.325 66.179 1.00 20.18 ATOM 2204 C4 LAT 1347 23.332 51.731 67.165 1.00 20.18 ATOM 2205 C5 LAT 1347 23.165 53.016 67.800 1.00 20.18 ATOM 2206 C6 LAT 1347 24.129 53.435 68.634 1.00 20.18 ATOM 2207 O1 LAT 1347 21.580 54.987 65.275 1.00 19.89 ATOM 2208 O2 LAT 1347 21.058 51.980 64.134 1.00 20.18 ATOM 2209 O3 LAT 1347 22.433 50.083 65.582 1.00 20.18 ATOM 2210 O5 LAT 1347 22.941 54.020 66.702 1.00 20.18 ATOM 2211 O6 LAT 1347 24.638 52.525 69.648 1.00 20.18 ATOM 2212 C1′ LAT 1347 20.888 59.061 65.028 1.00 19.89 ATOM 2213 C2′ LAT 1347 22.121 58.647 65.845 1.00 19.89 ATOM 2214 C3′ LAT 1347 22.505 57.214 65.448 1.00 19.89 ATOM 2215 C4′ LAT 1347 21.315 56.296 65.729 1.00 19.89 ATOM 2216 C5′ LAT 1347 20.008 56.750 65.020 1.00 19.89 ATOM 2217 C6′ LAT 1347 18.753 55.952 65.464 1.00 19.89 ATOM 2218 O1′ LAT 1347 20.572 60.386 65.395 1.00 19.89 ATOM 2219 O2′ LAT 1347 23.194 59.542 65.568 1.00 19.89 ATOM 2220 O3′ LAT 1347 23.637 56.854 66.255 1.00 19.89 ATOM 2221 O5′ LAT 1347 19.798 58.147 65.342 1.00 19.89 ATOM 2222 O6′ LAT 1347 18.292 55.063 64.439 1.00 19.89

[0496] TABLE 6 REMARK coordinates from minimization refinement REMARK refinement resolution: 20.0-2.0 A REMARK starting r = .1986 free_r = .2234 REMARK final  r = .1949 free_r = .2236 REMARK rmsd bonds = .006530 rmsd angles = 1.33814 REMARK wa = 1.2 REMARK target = mlf cycles = 1 steps = 20 REMARK sg = P2(1)2(1)2(1) a = 39.953 b = 76.126 c = 87.163 alpha = 90 beta = 90 gamma = 90 REMARK parameter file 1: CNS_TOPPAR:protein_rep.param REMARK parameter file 2: ../rnd5/upg.par REMARK parameter file 3: CNS_TOPPAR:ion.param REMARK parameter file 4: CNS_TOPPAR:water_rep.param REMARK parameter file 5: ../lat.par REMARK molecular structure file: generate8_2.mtf REMARK input coordinates: generate8_2.pdb REMARK reflection file = ../lac1.cv REMARK ncs = none REMARK B-correction resolution: 6.0-2.0 REMARK initial B-factor correction applied to fobs: REMARK  B11 = 2.769 B22 = 1.768 B33 = −4.536 REMARK  B12 =  .000 B13 =  .000 B23 =  .000 REMARK B-factor correction applied to coordinate array B: .038 REMARK bulk solvent: density level = .333397 e/A{fraction ( )}3, B-factor = 34.3204 A{fraction ( )}2 REMARK reflections with |Fobs|/sigma_F <0.0 rejected REMARK reflections with |Fobs| > 10000 * rms (Fobs) rejected REMARK theoretical total number of refl. in resol. range: 18567 ( 100.0% ) REMARK number of unobserved reflections (no entry or |F| = 0): 337 (  1.8% ) REMARK number of reflections rejected: 0 (  .0% ) REMARK total number of reflections used: 18230 ( 98.2% ) REMARK number of reflections in working set: 17343 ( 93.4% ) REMARK number of reflections in test set: 887 (  4.8% ) CRYST1  39.953  76.126  87.163  90.00 90.00 90.00 P 21 21 21 REMARK FILENAME = “minimize8_2.pdb” REMARK DATE: 8-Nov-00 23:09:42 created by user: karina REMARK VERSION: 1.0 ATOM 1 CB MSE 1 48.127 46.242 65.128 1.00 17.58 DIC ATOM 2 CG MSE 1 47.640 47.179 64.037 1.00 20.74 DIC ATOM 3 SE MSE 1 46.763 48.808 64.758 1.00 18.31 DIC ATOM 4 CE MSE 1 48.354 49.664 65.452 1.00 19.80 DIC ATOM 5 C MSE 1 47.777 44.093 63.871 1.00 13.39 DIC ATOM 6 O MSE 1 47.840 44.063 62.643 1.00 13.12 DIC ATOM 7 N MSE 1 49.999 45.167 63.882 1.00 14.29 DIC ATOM 8 CA MSE 1 48.769 44.914 64.676 1.00 14.05 DIC ATOM 9 N ASP 2 46.876 43.408 64.566 1.00 13.55 DIC ATOM 10 CA ASP 2 45.870 42.590 63.901 1.00 13.67 DIC ATOM 11 CB ASP 2 45.770 41.211 64.547 1.00 14.41 DIC ATOM 12 CG ASP 2 47.030 40.392 64.352 1.00 15.71 DIC ATOM 13 OD1 ASP 2 47.932 40.477 65.207 1.00 14.07 DIC ATOM 14 OD2 ASP 2 47.121 39.682 63.329 1.00 16.48 DIC ATOM 15 C ASP 2 44.519 43.273 63.942 1.00 14.09 DIC ATOM 16 O ASP 2 43.974 43.544 65.012 1.00 13.05 DIC ATOM 17 N ILE 3 43.994 43.562 62.758 1.00 12.65 DIC ATOM 18 CA ILE 3 42.707 44.217 62.624 1.00 11.17 DIC ATOM 19 CB ILE 3 42.748 45.331 61.560 1.00 10.15 DIC ATOM 20 CG2 ILE 3 41.355 45.938 61.402 1.00 8.26 DIC ATOM 21 CG1 ILE 3 43.816 46.371 61.921 1.00 9.18 DIC ATOM 22 CD ILE 3 43.553 47.140 63.221 1.00 10.15 DIC ATOM 23 C ILE 3 41.699 43.186 62.169 1.00 11.33 DIC ATOM 24 O ILE 3 42.021 42.313 61.364 1.00 12.76 DIC ATOM 25 N VAL 4 40.481 43.293 62.682 1.00 11.00 DIC ATOM 26 CA VAL 4 39.420 42.375 62.305 1.00 11.29 DIC ATOM 27 CB VAL 4 38.923 41.545 63.501 1.00 12.03 DIC ATOM 28 CG1 VAL 4 37.776 40.629 63.046 1.00 13.87 DIC ATOM 29 CG2 VAL 4 40.068 40.719 64.083 1.00 12.49 DIC ATOM 30 C VAL 4 38.226 43.144 61.758 1.00 10.90 DIC ATOM 31 O VAL 4 37.808 44.146 62.332 1.00 12.17 DIC ATOM 32 N PHE 5 37.704 42.676 60.630 1.00 11.30 DIC ATOM 33 CA PHE 5 36.524 43.259 59.998 1.00 9.47 DIC ATOM 34 CB PHE 5 36.862 43.876 58.635 1.00 11.11 DIC ATOM 35 CG PHE 5 37.513 45.229 58.702 1.00 9.37 DIC ATOM 36 CD1 PHE 5 36.818 46.332 59.186 1.00 10.57 DIC ATOM 37 CD2 PHE 5 38.799 45.412 58.204 1.00 10.04 DIC ATOM 38 CE1 PHE 5 37.398 47.610 59.164 1.00 11.62 DIC ATOM 39 CE2 PHE 5 39.386 46.674 58.178 1.00 11.49 DIC ATOM 40 CZ PHE 5 38.683 47.776 58.657 1.00 12.84 DIC ATOM 41 C PHE 5 35.589 42.074 59.748 1.00 10.75 DIC ATOM 42 O PHE 5 36.034 40.922 59.713 1.00 9.51 DIC ATOM 43 N ALA 6 34.305 42.364 59.581 1.00 8.88 DIC ATOM 44 CA ALA 6 33.296 41.353 59.281 1.00 9.05 DIC ATOM 45 CB ALA 6 32.408 41.090 60.493 1.00 7.20 DIC ATOM 46 C ALA 6 32.461 41.947 58.154 1.00 10.16 DIC ATOM 47 O ALA 6 32.012 43.093 58.247 1.00 9.64 DIC ATOM 48 N ALA 7 32.244 41.184 57.093 1.00 9.74 DIC ATOM 49 CA ALA 7 31.451 41.699 55.987 1.00 11.40 DIC ATOM 50 CB ALA 7 32.306 42.623 55.126 1.00 10.99 DIC ATOM 51 C ALA 7 30.852 40.616 55.113 1.00 11.73 DIC ATOM 52 O ALA 7 31.415 39.528 54.987 1.00 11.58 DIC ATOM 53 N ASP 8 29.686 40.914 54.542 1.00 11.95 DIC ATOM 54 CA ASP 8 29.040 40.005 53.609 1.00 10.87 DIC ATOM 55 CB ASP 8 27.516 39.942 53.812 1.00 11.16 DIC ATOM 56 CG ASP 8 26.892 41.297 54.079 1.00 11.92 DIC ATOM 57 OD1 ASP 8 27.415 42.320 53.585 1.00 9.02 DIC ATOM 58 OD2 ASP 8 25.855 41.326 54.779 1.00 12.31 DIC ATOM 59 C ASP 8 29.377 40.605 52.249 1.00 12.11 DIC ATOM 60 O ASP 8 30.072 41.621 52.176 1.00 12.03 DIC ATOM 61 N ASP 9 28.895 40.006 51.170 1.00 12.52 DIC ATOM 62 CA ASP 9 29.232 40.523 49.849 1.00 13.97 DIC ATOM 63 CB ASP 9 28.640 39.630 48.759 1.00 15.00 DIC ATOM 64 CG ASP 9 29.274 39.883 47.412 1.00 15.24 DIC ATOM 65 OD1 ASP 9 30.490 39.628 47.269 1.00 16.40 DIC ATOM 66 OD2 ASP 9 28.567 40.349 46.502 1.00 19.30 DIC ATOM 67 C ASP 9 28.808 41.970 49.613 1.00 14.35 DIC ATOM 68 O ASP 9 29.514 42.727 48.948 1.00 14.40 DIC ATOM 69 N ASN 10 27.660 42.352 50.164 1.00 14.55 DIC ATOM 70 CA ASN 10 27.135 43.704 50.010 1.00 15.08 DIC ATOM 71 CB ASN 10 25.792 43.817 50.738 1.00 15.92 DIC ATOM 72 CG ASN 10 25.151 45.191 50.593 1.00 16.37 DIC ATOM 73 OD1 ASN 10 24.987 45.697 49.486 1.00 15.05 DIC ATOM 74 ND2 ASN 10 24.772 45.791 51.719 1.00 15.34 DIC ATOM 75 C ASN 10 28.084 44.796 50.513 1.00 15.42 DIC ATOM 76 O ASN 10 28.065 45.922 50.007 1.00 14.99 DIC ATOM 77 N TYR 11 28.918 44.468 51.496 1.00 14.68 DIC, ATOM 78 CA TYR 11 29.846 45.453 52.063 1.00 13.78 DIC ATOM 79 CB TYR 11 29.746 45.436 53.592 1.00 13.14 DIC ATOM 80 CG TYR 11 28.744 46.423 54.138 1.00 15.36 DIC ATOM 81 CD1 TYR 11 27.647 46.820 53.376 1.00 15.46 DIC ATOM 82 CE1 TYR 11 26.735 47.745 53.859 1.00 16.70 DIC ATOM 83 CD2 TYR 11 28.900 46.976 55.409 1.00 15.54 DIC ATOM 84 CE2 TYR 11 27.988 47.902 55.904 1.00 18.09 DIC ATOM 85 CZ TYR 11 26.909 48.281 55.120 1.00 17.62 DIC ATOM 86 OH TYR 11 26.005 49.200 55.585 1.00 19.94 DIC ATOM 87 C TYR 11 31.300 45.295 51.647 1.00 13.79 DIC ATOM 88 O TYR 11 32.183 45.965 52.193 1.00 13.61 DIC ATOM 89 N ALA 12 31.553 44.428 50.672 1.00 13.51 DIC ATOM 90 CA ALA 12 32.917 44.197 50.211 1.00 13.12 DIC ATOM 91 CB ALA 12 32.929 43.146 49.089 1.00 13.34 DIC ATOM 92 C ALA 12 33.604 45.484 49.736 1.00 11.96 DIC ATOM 93 O ALA 12 34.774 45.713 50.038 1.00 9.55 DIC ATOM 94 N ALA 13 32.888 46.325 48.995 1.00 11.10 DIC ATOM 95 CA ALA 13 33.491 47.565 48.499 1.00 11.93 DIC ATOM 96 CB ALA 13 32.550 48.251 47.499 1.00 10.97 DIC ATOM 97 C ALA 13 33.832 48.507 49.660 1.00 11.31 DIC ATOM 98 O ALA 13 34.914 49.097 49.700 1.00 12.37 DIC ATOM 99 N TYR 14 32.915 48.625 50.613 1.00 12.09 DIC ATOM 100 CA TYR 14 33.114 49.479 51.782 1.00 10.69 DIC ATOM 101 CB TYR 14 31.813 49.571 52.590 1.00 10.74 DIC ATOM 102 CG TYR 14 30.615 49.952 51.743 1.00 13.01 DIC ATOM 103 CD1 TYR 14 30.753 50.842 50.677 1.00 12.55 DIC ATOM 104 CE1 TYR 14 29.669 51.210 49.896 1.00 13.46 DIC ATOM 105 CD2 TYR 14 29.347 49.434 52.010 1.00 13.02 DIC ATOM 106 CE2 TYR 14 28.245 49.799 51.232 1.00 16.28 DIC ATOM 107 CZ TYR 14 28.424 50.693 50.176 1.00 16.05 DIC ATOM 108 OH TYR 14 27.358 51.101 49.416 1.00 19.24 DIC ATOM 109 C TYR 14 34.246 48.951 52.659 1.00 10.96 DIC ATOM 110 O TYR 14 35.013 49.730 53.237 1.00 10.92 DIC ATOM 111 N LEU 15 34.339 47.626 52.770 1.00 10.75 DIC ATOM 112 CA LEU 15 35.396 46.994 53.550 1.00 10.52 DIC ATOM 113 CB LEU 15 35.303 45.466 53.434 1.00 11.98 DIC ATOM 114 CG LEU 15 36.572 44.675 53.789 1.00 14.65 DIC ATOM 115 CD1 LEU 15 36.856 44.790 55.290 1.00 15.28 DIC ATOM 116 CD2 LEU 15 36.396 43.209 53.395 1.00 13.71 DIC ATOM 117 C LEU 15 36.751 47.458 53.010 1.00 10.20 DIC ATOM 118 O LEU 15 37.645 47.823 53.771 1.00 10.38 DIC ATOM 119 N CYS 16 36.896 47.424 51.686 1.00 12.12 DIC ATOM 120 CA CYS 16 38.136 47.838 51.038 1.00 11.09 DIC ATOM 121 CB CYS 16 37.997 47.725 49.515 1.00 12.05 DIC ATOM 122 SG CYS 16 39.517 48.138 48.641 1.00 12.15 DIC ATOM 123 C CYS 16 38.519 49.274 51.415 1.00 10.93 DIC ATOM 124 O CYS 16 39.671 49.550 51.757 1.00 11.30 DIC ATOM 125 N VAL 17 37.553 50.185 51.353 1.00 10.79 DIC ATOM 126 CA VAL 17 37.805 51.585 51.695 1.00 12.24 DIC ATOM 127 CB VAL 17 36.549 52.448 51.438 1.00 12.01 DIC ATOM 128 CG1 VAL 17 36.734 53.840 52.022 1.00 11.58 DIC ATOM 129 CG2 VAL 17 36.282 52.531 49.929 1.00 12.39 DIC ATOM 130 C VAL 17 38.231 51.720 53.159 1.00 12.59 DIC ATOM 131 O VAL 17 39.192 52.422 53.478 1.00 14.20 DIC ATOM 132 N ALA 18 37.517 51.038 54.045 1.00 12.29 DIC ATOM 133 CA ALA 18 37.831 51.084 55.470 1.00 11.27 DIC ATOM 134 CB ALA 18 36.816 50.262 56.247 1.00 11.41 DIC ATOM 135 C ALA 18 39.237 50.539 55.723 1.00 12.12 DIC ATOM 136 O ALA 18 40.018 51.123 56.479 1.00 9.33 DIC ATOM 137 N ALA 19 39.545 49.416 55.081 1.00 11.56 DIC ATOM 138 CA ALA 19 40.840 48.772 55.234 1.00 12.42 DIC ATOM 139 CB ALA 19 40.883 47.481 54.418 1.00 12.78 DIC ATOM 140 C ALA 19 41.966 49.705 54.806 1.00 13.64 DIC ATOM 141 O ALA 19 42.970 49.834 55.507 1.00 12.89 DIC ATOM 142 N LYS 20 41.805 50.362 53.661 1.00 14.08 DIC ATOM 143 CA LYS 20 42.836 51.279 53.202 1.00 14.66 DIC ATOM 144 CB LYS 20 42.532 51.789 51.793 1.00 15.85 DIC ATOM 145 CG LYS 20 43.694 52.575 51.192 1.00 20.09 DIC ATOM 146 CD LYS 20 43.502 52.849 49.706 1.00 22.70 DIC ATOM 147 CE LYS 20 44.681 53.638 49.161 1.00 22.43 DIC ATOM 148 NZ LYS 20 44.540 53.943 47.712 1.00 24.73 DIC ATOM 149 C LYS 20 42.993 52.458 54.162 1.00 14.30 DIC ATOM 150 O LYS 20 44.098 52.980 54.329 1.00 13.09 DIC ATOM 151 N SER 21 41.906 52.883 54.809 1.00 13.25 DIC ATOM 152 CA SER 21 42.033 54.003 55.741 1.00 12.72 DIC ATOM 153 CB SER 21 40.660 54.440 56.283 1.00 12.54 DIC ATOM 154 OG SER 21 40.244 53.667 57.395 1.00 12.59 DIC ATOM 155 C SER 21 42.962 53.586 56.886 1.00 12.00 DIC ATOM 156 O SER 21 43.748 54.387 57.392 1.00 13.07 DIC ATOM 157 N VAL 22 42.890 52.319 57.279 1.00 11.25 DIC ATOM 158 CA VAL 22 43.747 51.816 58.348 1.00 11.30 DIC ATOM 159 CB VAL 22 43.360 50.374 58.752 1.00 11.76 DIC ATOM 160 CG1 VAL 22 44.298 49.870 59.821 1.00 11.30 DIC ATOM 161 CG2 VAL 22 41.921 50.339 59.241 1.00 11.48 DIC ATOM 162 C VAL 22 45.212 51.814 57.912 1.00 11.89 DIC ATOM 163 O VAL 22 46.095 52.246 58.662 1.00 12.69 DIC ATOM 164 N GLU 23 45.478 51.328 56.704 1.00 10.93 DIC ATOM 165 CA GLU 23 46.854 51.295 56.219 1.00 13.03 DIC ATOM 166 CB GLU 23 46.952 50.615 54.849 1.00 14.30 DIC ATOM 167 CG GLU 23 46.544 49.160 54.823 1.00 14.62 DIC ATOM 168 CD GLU 23 46.836 48.512 53.480 1.00 16.61 DIC ATOM 169 OE1 GLU 23 46.678 49.196 52.449 1.00 17.40 DIC ATOM 170 OE2 GLU 23 47.209 47.317 53.453 1.00 16.65 DIC ATOM 171 C GLU 23 47.407 52.707 56.104 1.00 12.51 DIC ATOM 172 O GLU 23 48.538 52.969 56.502 1.00 14.38 DIC ATOM 173 N ALA 24 46.603 53.620 55.572 1.00 11.76 DIC ATOM 174 CA ALA 24 47.046 54.997 55.397 1.00 12.06 DIC ATOM 175 CB ALA 24 45.945 55.827 54.716 1.00 11.87 DIC ATOM 176 C ALA 24 47.445 55.635 56.722 1.00 11.80 DIC ATOM 177 O ALA 24 48.393 56.425 56.775 1.00 11.54 DIC ATOM 178 N ALA 25 46.734 55.279 57.789 1.00 11.43 DIC ATOM 179 CA ALA 25 47.005 55.825 59.123 1.00 11.35 DIC ATOM 180 CB ALA 25 45.757 55.698 59.998 1.00 11.07 DIC ATOM 181 C ALA 25 48.194 55.180 59.836 1.00 11.54 DIC ATOM 182 O ALA 25 48.596 55.630 60.904 1.00 10.97 DIC ATOM 183 N HIS 26 48.753 54.123 59.264 1.00 11.65 DIC ATOM 184 CA HIS 26 49.899 53.464 59.893 1.00 13.56 DIC ATOM 185 CB HIS 26 49.452 52.198 60.628 1.00 13.72 DIC ATOM 186 CG HIS 26 48.350 52.425 61.617 1.00 14.14 DIC ATOM 187 CD2 HIS 26 48.381 52.626 62.958 1.00 13.28 DIC ATOM 188 ND1 HIS 26 47.020 52.455 61.255 1.00 11.89 DIC ATOM 189 CE1 HIS 26 46.277 52.660 62.330 1.00 12.65 DIC ATOM 190 NE2 HIS 26 47.078 52.768 63.375 1.00 14.11 DIC ATOM 191 C HIS 26 50.940 53.111 58.833 1.00 13.66 DIC ATOM 192 O HIS 26 51.151 51.941 58.512 1.00 13.39 DIC ATOM 193 N PRO 27 51.615 54.132 58.284 1.00 14.55 DIC ATOM 194 CD PRO 27 51.529 55.536 58.728 1.00 15.30 DIC ATOM 195 CA PRO 27 52.640 53.966 57.247 1.00 14.85 DIC ATOM 196 CB PRO 27 53.078 55.408 56.957 1.00 16.08 DIC ATOM 197 CG PRO 27 52.856 56.104 58.270 1.00 17.10 DIC ATOM 198 C PRO 27 53.810 53.046 57.592 1.00 15.06 DIC ATOM 199 O PRO 27 54.397 52.425 56.696 1.00 15.60 DIC ATOM 200 N ASP 28 54.149 52.936 58.874 1.00 13.42 DIC ATOM 201 CA ASP 28 55.265 52.074 59.251 1.00 13.91 DIC ATOM 202 CB ASP 28 56.401 52.896 59.867 1.00 12.65 DIC ATOM 203 CG ASP 28 57.698 52.099 59.970 1.00 13.98 DIC ATOM 204 OD1 ASP 28 58.008 51.345 59.017 1.00 14.45 DIC ATOM 205 OD2 ASP 28 58.405 52.229 60.988 1.00 11.69 DIC ATOM 206 C ASP 28 54.879 50.946 60.197 1.00 13.78 DIC ATOM 207 O ASP 28 55.708 50.445 60.950 1.00 13.88 DIC ATOM 208 N THR 29 53.617 50.546 60.160 1.00 14.27 DIC ATOM 209 CA THR 29 53.166 49.457 61.011 1.00 15.21 DIC ATOM 210 CB THR 29 52.082 49.917 62.001 1.00 15.30 DIC ATOM 211 OG1 THR 29 52.567 51.025 62.772 1.00 15.73 DIC ATOM 212 CG2 THR 29 51.732 48.782 62.948 1.00 17.03 DIC ATOM 213 C THR 29 52.594 48.339 60.149 1.00 15.61 DIC ATOM 214 O THR 29 51.884 48.596 59.176 1.00 14.30 DIC ATOM 215 N GLU 30 52.927 47.101 60.499 1.00 16.81 DIC ATOM 216 CA GLU 30 52.427 45.936 59.779 1.00 17.79 DIC ATOM 217 CB GLU 30 53.187 44.680 60.215 1.00 21.66 DIC ATOM 218 CG GLU 30 53.405 43.645 59.115 1.00 28.54 DIC ATOM 219 CD GLU 30 54.135 44.217 57.900 1.00 29.87 DIC ATOM 220 OE1 GLU 30 53.472 44.811 57.024 1.00 31.57 DIC ATOM 221 OE2 GLU 30 55.375 44.084 57.826 1.00 33.06 DIC ATOM 222 C GLU 30 50.957 45.790 60.147 1.00 16.87 DIC ATOM 223 O GLU 30 50.617 45.687 61.325 1.00 17.37 DIC ATOM 224 N ILE 31 50.082 45.800 59.151 1.00 15.55 DIC ATOM 225 CA ILE 31 48.658 45.652 59.418 1.00 15.24 DIC ATOM 226 CB ILE 31 47.821 46.802 58.782 1.00 14.65 DIC ATOM 227 CG2 ILE 31 46.341 46.638 59.150 1.00 15.64 DIC ATOM 228 CG1 ILE 31 48.323 48.163 59.278 1.00 14.25 DIC ATOM 229 CD ILE 31 48.159 48.389 60.765 1.00 15.14 DIC ATOM 230 C ILE 31 48.188 44.319 58.849 1.00 14.29 DIC ATOM 231 O ILE 31 48.129 44.132 57.634 1.00 14.29 DIC ATOM 232 N ARG 32 47.877 43.386 59.739 1.00 13.00 DIC ATOM 233 CA ARG 32 47.398 42.081 59.328 1.00 12.73 DIC ATOM 234 CB ARG 32 48.045 40.984 60.182 1.00 15.39 DIC ATOM 235 CG ARG 32 49.580 40.988 60.101 1.00 21.06 DIC ATOM 236 CD ARG 32 50.221 39.798 60.809 1.00 25.85 DIC ATOM 237 NE ARG 32 49.830 39.700 62.216 1.00 31.82 DIC ATOM 238 CZ ARG 32 50.327 38.808 63.069 1.00 35.29 DIC ATOM 239 NH1 ARG 32 51.246 37.938 62.657 1.00 36.77 DIC ATOM 240 NH2 ARG 32 49.897 38.772 64.329 1.00 34.04 DIC ATOM 241 C ARG 32 45.884 42.079 59.487 1.00 11.59 DIC ATOM 242 O ARG 32 45.365 42.130 60.604 1.00 10.59 DIC ATOM 243 N PHE 33 45.190 42.061 58.353 1.00 9.57 DIC ATOM 244 CA PHE 33 43.733 42.059 58.314 1.00 11.07 DIC ATOM 245 CB PHE 33 43.233 42.709 57.021 1.00 9.65 DIC ATOM 246 CG PHE 33 43.473 44.187 56.942 1.00 9.60 DIC ATOM 247 CD1 PHE 33 42.751 45.069 57.741 1.00 8.83 DIC ATOM 248 CD2 PHE 33 44.394 44.703 56.034 1.00 10.43 DIC ATOM 249 CE1 PHE 33 42.939 46.449 57.634 1.00 9.43 DIC. ATOM 250 CE2 PHE 33 44.590 46.078 55.918 1.00 9.57 DIC ATOM 251 CZ PHE 33 43.861 46.953 56.718 1.00 9.32 DIC ATOM 252 C PHE 33 43.142 40.652 58.391 1.00 11.46 DIC ATOM 253 O PHE 33 43.577 39.741 57.678 1.00 12.46 DIC ATOM 254 N HIS 34 42.138 40.495 59.246 1.00 10.60 DIC ATOM 255 CA HIS 34 41.437 39.222 59.414 1.00 12.40 DIC ATOM 256 CB HIS 34 41.567 38.728 60.859 1.00 11.10 DIC ATOM 257 CG HIS 34 42.983 38.591 61.328 1.00 12.97 DIC ATOM 258 CD2 HIS 34 43.844 39.503 61.841 1.00 12.88 DIC ATOM 259 ND1 HIS 34 43.667 37.394 61.300 1.00 14.47 DIC ATOM 260 CE1 HIS 34 44.887 37.574 61.776 1.00 14.13 DIC ATOM 261 NE2 HIS 34 45.019 38.845 62.113 1.00 14.30 DIC ATOM 262 C HIS 34 39.978 39.545 59.103 1.00 12.39 DIC ATOM 263 O HIS 34 39.337 40.294 59.840 1.00 12.46 DIC ATOM 264 N VAL 35 39.449 38.987 58.019 1.00 10.81 DIC ATOM 265 CA VAL 35 38.073 39.280 57.643 1.00 10.52 DIC ATOM 266 CB VAL 35 37.991 39.696 56.150 1.00 11.67 DIC ATOM 267 CG1 VAL 35 36.571 40.115 55.793 1.00 12.07 DIC ATOM 268 CG2 VAL 35 38.970 40.838 55.875 1.00 11.00 DIC ATOM 269 C VAL 35 37.088 38.141 57.878 1.00 11.06 DIC ATOM 270 O VAL 35 37.229 37.055 57.307 1.00 10.52 DIC ATOM 271 N LEU 36 36.096 38.391 58.730 1.00 10.89 DIC ATOM 272 CA LEU 36 35.057 37.401 58.994 1.00 11.46 DIC ATOM 273 CB LEU 36 34.272 37.769 60.262 1.00 11.18 DIC ATOM 274 CG LEU 36 35.134 37.949 61.527 1.00 11.27 DIC ATOM 275 CD1 LEU 36 34.224 38.089 62.748 1.00 10.72 DIC ATOM 276 CD2 LEU 36 36.061 36.750 61.721 1.00 9.09 DIC ATOM 277 C LEU 36 34.201 37.528 57.732 1.00 12.89 DIC ATOM 278 O LEU 36 33.465 38.501 57.556 1.00 11.93 DIC ATOM 279 N ASP 37 34.351 36.547 56.845 1.00 14.29 DIC ATOM 280 CA ASP 37 33.694 36.513 55.538 1.00 14.87 DIC ATOM 281 CB ASP 37 34.654 35.854 54.538 1.00 17.19 DIC ATOM 282 CG ASP 37 34.122 35.845 53.120 1.00 15.95 DIC ATOM 283 OD1 ASP 37 32.917 36.093 52.917 1.00 16.13 DIC ATOM 284 OD2 ASP 37 34.920 35.571 52.207 1.00 19.63 DIC ATOM 285 C ASP 37 32.362 35.774 55.545 1.00 16.83 DIC ATOM 286 O ASP 37 32.320 34.539 55.625 1.00 14.89 DIC ATOM 287 N ALA 38 31.275 36.531 55.429 1.00 15.59 DIC ATOM 288 CA ALA 38 29.947 35.941 55.447 1.00 18.57 DIC ATOM 289 CB ALA 38 29.010 36.795 56.307 1.00 19.77 DIC ATOM 290 C ALA 38 29.330 35.719 54.069 1.00 19.75 DIC ATOM 291 O ALA 38 28.111 35.689 53.937 1.00 23.40 DIC ATOM 292 N GLY 39 30.161 35.560 53.045 1.00 19.13 DIC ATOM 293 CA GLY 39 29.627 35.321 51.717 1.00 17.91 DIC ATOM 294 C GLY 39 30.163 36.247 50.641 1.00 16.51 DIC ATOM 295 O GLY 39 29.486 36.494 49.649 1.00 18.04 DIC ATOM 296 N ILE 40 31.371 36.768 50.832 1.00 14.45 DIC ATOM 297 CA ILE 40 31.975 37.662 49.848 1.00 14.34 DIC ATOM 298 CB ILE 40 33.195 38.400 50.450 1.00 13.99 DIC ATOM 299 CG2 ILE 40 33.718 39.424 49.460 1.00 13.81 DIC ATOM 300 CG1 ILE 40 32.788 39.096 51.760 1.00 13.39 DIC ATOM 301 CD ILE 40 33.946 39.762 52.517 1.00 13.39 DIC ATOM 302 C ILE 40 32.407 36.846 48.621 1.00 14.46 DIC ATOM 303 O ILE 40 33.064 35.817 48.751 1.00 14.76 DIC ATOM 304 N SER 41 32.029 37.299 47.429 1.00 14.97 DIC ATOM 305 CA SER 41 32.376 36.573 46.207 1.00 15.36 DIC ATOM 306 CB SER 41 31.711 37.221 44.987 1.00 15.16 DIC ATOM 307 OG SER 41 32.356 38.436 44.642 1.00 14.14 DIC ATOM 308 C SER 41 33.880 36.531 45.988 1.00 16.18 DIC ATOM 309 O SER 41 34.615 37.374 46.504 1.00 17.61 DIC ATOM 310 N GLU 42 34.334 35.546 45.219 1.00 16.89 DIC ATOM 311 CA GLU 42 35.754 35.406 44.922 1.00 16.48 DIC ATOM 312 CB GLU 42 36.008 34.191 44.018 1.00 18.56 DIC ATOM 313 CG GLU 42 37.468 34.005 43.605 1.00 20.32 DIC ATOM 314 CD GLU 42 37.919 34.923 42.467 1.00 24.54 DIC ATOM 315 OE1 GLU 42 39.149 35.117 42.326 1.00 27.22 DIC ATOM 316 OE2 GLU 42 37.064 35.440 41.707 1.00 24.68 DIC ATOM 317 C GLU 42 36.249 36.654 44.217 1.00 15.88 DIC ATOM 318 O GLU 42 37.381 37.083 44.423 1.00 14.39 DIC ATOM 319 N ALA 43 35.399 37.234 43.378 1.00 17.03 DIC ATOM 320 CA ALA 43 35.792 38.427 42.640 1.00 17.82 DIC ATOM 321 CB ALA 43 34.752 38.758 41.562 1.00 18.48 DIC ATOM 322 C ALA 43 35.966 39.605 43.587 1.00 16.49 DIC ATOM 323 O ALA 43 36.898 40.396 43.440 1.00 15.18 DIC ATOM 324 N ASN 44 35.086 39.717 44.574 1.00 15.20 DIC ATOM 325 CA ASN 44 35.200 40.836 45.500 1.00 16.12 DIC ATOM 326 CB ASN 44 33.880 41.055 46.248 1.00 15.18 DIC ATOM 327 CG ASN 44 32.838 41.754 45.385 1.00 19.28 DIC ATOM 328 OD1 ASN 44 33.171 42.636 44.586 1.00 19.46 DIC ATOM 329 ND2 ASN 44 31.571 41.378 45.551 1.00 18.90 DIC ATOM 330 C ASN 44 36.372 40.684 46.470 1.00 15.26 DIC ATOM 331 O ASN 44 36.961 41.673 46.888 1.00 15.20 DIC ATOM 332 N ARG 45 36.724 39.449 46.817 1.00 16.07 DIC ATOM 333 CA ARG 45 37.851 39.234 47.712 1.00 16.99 DIC ATOM 334 CB ARG 45 37.909 37.769 48.167 1.00 19.65 DIC ATOM 335 CG ARG 45 36.581 37.274 48.728 1.00 24.95 DIC ATOM 336 CD ARG 45 36.731 36.329 49.909 1.00 30.41 DIC ATOM 337 NE ARG 45 37.494 35.125 49.592 1.00 34.93 DIC ATOM 338 CZ ARG 45 37.562 34.059 50.387 1.00 38.05 DIC ATOM 339 NH1 ARG 45 36.907 34.046 51.542 1.00 39.62 DIC ATOM 340 NH2 ARG 45 38.294 33.007 50.037 1.00 39.66 DIC ATOM 341 C ARG 45 39.128 39.620 46.963 1.00 16.64 DIC ATOM 342 O ARG 45 40.009 40.267 47.522 1.00 15.53 DIC ATOM 343 N ALA 46 39.218 39.242 45.690 1.00 14.76 DIC ATOM 344 CA ALA 46 40.396 39.582 44.901 1.00 15.52 DIC ATOM 345 CB ALA 46 40.321 38.933 43.514 1.00 16.34 DIC ATOM 346 C ALA 46 40.499 41.099 44.763 1.00 15.93 DIC ATOM 347 O ALA 46 41.581 41.669 44.890 1.00 16.56 DIC ATOM 348 N ALA 47 39.367 41.753 44.514 1.00 15.64 DIC ATOM 349 CA ALA 47 39.358 43.204 44.355 1.00 15.26 DIC ATOM 350 CB ALA 47 37.985 43.671 43.903 1.00 14.76 DIC ATOM 351 C ALA 47 39.762 43.918 45.643 1.00 14.97 DIC ATOM 352 O ALA 47 40.498 44.897 45.612 1.00 15.32 DIC ATOM 353 N VAL 48 39.274 43.435 46.781 1.00 14.13 DIC ATOM 354 CA VAL 48 39.632 44.054 48.048 1.00 12.62 DIC ATOM 355 CB VAL 48 38.887 43.393 49.229 1.00 11.63 DIC ATOM 356 CG1 VAL 48 39.427 43.922 50.543 1.00 10.65 DIC ATOM 357 CG2 VAL 48 37.391 43.675 49.127 1.00 10.00 DIC ATOM 358 C VAL 48 41.142 43.927 48.271 1.00 13.29 DIC ATOM 359 O VAL 48 41.810 44.899 48.612 1.00 12.89 DIC ATOM 360 N ALA 49 41.676 42.726 48.062 1.00 13.20 DIC ATOM 361 CA ALA 49 43.099 42.476 48.257 1.00 15.72 DIC ATOM 362 CB ALA 49 43.389 40.974 48.140 1.00 14.62 DIC ATOM 363 C ALA 49 43.977 43.255 47.282 1.00 17.17 DIC ATOM 364 O ALA 49 45.025 43.776 47.666 1.00 18.51 DIC ATOM 365 N ALA 50 43.549 43.342 46.026 1.00 17.97 DIC ATOM 366 CA ALA 50 44.321 44.057 45.012 1.00 19.51 DIC ATOM 367 CB ALA 50 43.651 43.915 43.643 1.00 19.91 DIC ATOM 368 C ALA 50 44.514 45.539 45.335 1.00 19.92 DIC ATOM 369 O ALA 50 45.414 46.178 44.796 1.00 20.21 DIC ATOM 370 N ASN 51 43.666 46.089 46.200 1.00 19.48 DIC ATOM 371 CA ASN 51 43.770 47.505 46.565 1.00 18.23 DIC ATOM 372 CB ASN 51 42.379 48.125 46.722 1.00 16.61 DIC ATOM 373 CG ASN 51 41.690 48.369 45.391 1.00 17.51 DIC ATOM 374 OD1 ASN 51 42.160 49.161 44.577 1.00 18.25 DIC ATOM 375 ND2 ASN 51 40.570 47.689 45.165 1.00 15.70 DIC ATOM 376 C ASN 51 44.551 47.733 47.855 1.00 18.98 DIC ATOM 377 O ASN 51 44.802 48.877 48.241 1.00 18.73 DIC ATOM 378 N LEU 52 44.929 46.657 48.533 1.00 18.72 DIC ATOM 379 CA LEU 52 45.671 46.812 49.778 1.00 20.64 DIC ATOM 380 CB LEU 52 45.208 45.778 50.805 1.00 18.56 DIC ATOM 381 CG LEU 52 43.701 45.819 51.069 1.00 18.19 DIC ATOM 382 CD1 LEU 52 43.336 44.772 52.106 1.00 19.78 DIC ATOM 383 CD2 LEU 52 43.292 47.202 51.529 1.00 18.99 DIC ATOM 384 C LEU 52 47.171 46.702 49.554 1.00 22.97 DIC ATOM 385 O LEU 52 47.626 46.310 48.476 1.00 21.94 DIC ATOM 386 N ARG 53 47.931 47.057 50.583 1.00 24.82 DIC ATOM 387 CA ARG 53 49.387 47.024 50.523 1.00 28.21 DIC ATOM 388 CB ARG 53 49.966 47.479 51.878 1.00 27.92 DIC ATOM 389 CG ARG 53 50.738 48.796 51.811 1.00 26.01 DIC ATOM 390 CD ARG 53 50.572 49.669 53.069 1.00 26.38 DIC ATOM 391 NE ARG 53 50.831 48.945 54.310 1.00 21.46 DIC ATOM 392 CZ ARG 53 50.875 49.507 55.516 1.00 22.17 DIC ATOM 393 NH1 ARG 53 50.682 50.814 55.662 1.00 22.29 DIC ATOM 394 NH2 ARG 53 51.098 48.757 56.585 1.00 18.63 DIC ATOM 395 C ARG 53 49.931 45.650 50.136 1.00 29.98 DIC ATOM 396 O ARG 53 49.397 44.613 50.534 1.00 30.96 DIC ATOM 397 N GLY 54 50.989 45.655 49.333 1.00 32.74 DIC ATOM 398 CA GLY 54 51.606 44.414 48.903 1.00 34.79 DIC ATOM 399 C GLY 54 50.684 43.486 48.136 1.00 37.38 DIC ATOM 400 O GLY 54 50.848 42.263 48.190 1.00 37.61 DIC ATOM 401 N GLY 55 49.718 44.061 47.421 1.00 37.91 DIC ATOM 402 CA GLY 55 48.782 43.259 46.654 1.00 38.40 DIC ATOM 403 C GLY 55 47.822 42.468 47.526 1.00 38.63 DIC ATOM 404 O GLY 55 47.220 41.492 47.077 1.00 38.78 DIC ATOM 405 N GLY 56 47.678 42.887 48.779 1.00 38.50 DIC ATOM 406 CA GLY 56 46.780 42.198 49.685 1.00 38.47 DIC ATOM 407 C GLY 56 47.417 40.973 50.309 1.00 38.75 DIC ATOM 408 O GLY 56 46.747 39.964 50.534 1.00 40.02 DIC ATOM 409 N GLY 57 48.716 41.061 50.586 1.00 37.85 DIC ATOM 410 CA GLY 57 49.424 39.948 51.193 1.00 35.96 DIC ATOM 411 C GLY 57 49.144 39.855 52.682 1.00 34.60 DIC ATOM 412 O GLY 57 49.441 38.845 53.321 1.00 34.23 DIC ATOM 413 N ASN 58 48.568 40.914 53.241 1.00 33.21 DIC ATOM 414 CA ASN 58 48.250 40.933 54.664 1.00 31.01 DIC ATOM 415 CB ASN 58 48.877 42.154 55.328 1.00 33.87 DIC ATOM 416 CG ASN 58 50.322 41.922 55.706 1.00 37.81 DIC ATOM 417 OD1 ASN 58 50.618 41.127 56.604 1.00 38.68 DIC ATOM 418 ND2 ASN 58 51.234 42.603 55.016 1.00 39.42 DIC ATOM 419 C ASN 58 46.763 40.889 54.965 1.00 28.44 DIC ATOM 420 O ASN 58 46.279 41.588 55.861 1.00 25.75 DIC ATOM 421 N ILE 59 46.035 40.070 54.211 1.00 24.88 DIC ATOM 422 CA ILE 59 44.607 39.927 54.445 1.00 23.41 DIC ATOM 423 CB ILE 59 43.763 40.859 53.526 1.00 23.71 DIC ATOM 424 CG2 ILE 59 43.989 40.514 52.055 1.00 22.32 DIC ATOM 425 CG1 ILE 59 42.282 40.740 53.909 1.00 21.89 DIC ATOM 426 CD ILE 59 41.398 41.852 53.361 1.00 22.80 DIC ATOM 427 C ILE 59 44.167 38.482 54.264 1.00 22.27 DIC ATOM 428 O ILE 59 44.400 37.863 53.221 1.00 21.93 DIC ATOM 429 N ARG 60 43.550 37.945 55.308 1.00 20.40 DIC ATOM 430 CA ARG 60 43.062 36.574 55.300 1.00 19.40 DIC ATOM 431 CB ARG 60 43.748 35.769 56.417 1.00 20.70 DIC ATOM 432 CG ARG 60 43.338 34.300 56.513 1.00 25.16 DIC ATOM 433 CD ARG 60 44.461 33.403 57.069 1.00 29.20 DIC ATOM 434 NE ARG 60 44.896 33.763 58.418 1.00 33.94 DIC ATOM 435 CZ ARG 60 45.736 34.757 58.707 1.00 36.79 DIC ATOM 436 NH1 ARG 60 46.250 35.507 57.740 1.00 38.29 DIC ATOM 437 NH2 ARG 60 46.068 35.000 59.971 1.00 36.32 DIC ATOM 438 C ARG 60 41.554 36.613 55.508 1.00 18.67 DIC ATOM 439 O ARG 60 41.062 37.256 56.441 1.00 19.14 DIC ATOM 440 N PHE 61 40.820 35.959 54.615 1.00 15.54 DIC ATOM 441 CA PHE 61 39.369 35.904 54.722 1.00 16.16 DIC ATOM 442 CB PHE 61 38.713 35.924 53.333 1.00 14.93 DIC ATOM 443 CG PHE 61 38.885 37.230 52.601 1.00 12.73 DIC ATOM 444 CD1 PHE 61 39.989 37.448 51.786 1.00 13.77 DIC ATOM 445 CD2 PHE 61 37.958 38.258 52.763 1.00 11.24 DIC ATOM 446 CE1 PHE 61 40.170 38.677 51.143 1.00 14.58 DIC ATOM 447 CE2 PHE 61 38.128 39.482 52.131 1.00 12.41 DIC ATOM 448 CZ PHE 61 39.236 39.696 51.319 1.00 11.76 DIC ATOM 449 C PHE 61 39.026 34.613 55.448 1.00 16.95 DIC ATOM 450 O PHE 61 39.542 33.554 55.105 1.00 18.27 DIC ATOM 451 N ILE 62 38.176 34.714 56.467 1.00 17.58 DIC ATOM 452 CA ILE 62 37.767 33.560 57.264 1.00 16.19 DIC ATOM 453 CB ILE 62 38.022 33.809 58.770 1.00 16.81 DIC ATOM 454 CG2 ILE 62 37.808 32.521 59.560 1.00 15.43 DIC ATOM 455 CG1 ILE 62 39.443 34.321 58.987 1.00 17.10 DIC ATOM 456 CD ILE 62 39.684 34.852 60.390 1.00 19.03 DIC ATOM 457 C ILE 62 36.271 33.328 57.075 1.00 16.68 DIC ATOM 458 O ILE 62 35.456 34.150 57.495 1.00 13.95 DIC ATOM 459 N ASP 63 35.911 32.207 56.457 1.00 17.73 DIC ATOM 460 CA ASP 63 34.507 31.906 56.219 1.00 20.50 DIC ATOM 461 CB ASP 63 34.354 30.648 55.352 1.00 24.57 DIC ATOM 462 CG ASP 63 34.848 30.853 53.926 1.00 28.34 DIC ATOM 463 OD1 ASP 63 34.508 31.890 53.317 1.00 31.73 DIC ATOM 464 OD2 ASP 63 35.566 29.971 53.412 1.00 32.70 DIC ATOM 465 C ASP 63 33.716 31.723 57.504 1.00 20.66 DIC ATOM 466 O ASP 63 34.147 31.036 58.436 1.00 20.12 DIC ATOM 467 N VAL 64 32.557 32.363 57.549 1.00 20.64 DIC ATOM 468 CA VAL 64 31.662 32.254 58.686 1.00 20.45 DIC ATOM 469 CB VAL 64 31.601 33.569 59.498 1.00 22.06 DIC ATOM 470 CG1 VAL 64 32.985 33.917 60.013 1.00 22.97 DIC ATOM 471 CG2 VAL 64 31.056 34.696 58.645 1.00 22.72 DIC ATOM 472 C VAL 64 30.290 31.924 58.116 1.00 20.57 DIC ATOM 473 O VAL 64 29.936 32.377 57.024 1.00 20.54 DIC ATOM 474 N ASN 65 29.536 31.107 58.840 1.00 19.87 DIC ATOM 475 CA ASN 65 28.203 30.709 58.406 1.00 20.85 DIC ATOM 476 CB ASN 65 27.898 29.282 58.869 1.00 21.23 DIC ATOM 477 CG ASN 65 26.615 28.732 58.264 1.00 24.15 DIC ATOM 478 OD1 ASN 65 25.670 29.478 57.988 1.00 24.03 DIC ATOM 479 ND2 ASN 65 26.572 27.418 58.067 1.00 22.28 DIC ATOM 480 C ASN 65 27.195 31.666 59.034 1.00 21.32 DIC ATOM 481 O ASN 65 26.916 31.586 60.229 1.00 20.43 DIC ATOM 482 N PRO 66 26.625 32.575 58.231 1.00 21.57 DIC ATOM 483 CD PRO 66 26.755 32.695 56.768 1.00 22.50 DIC ATOM 484 CA PRO 66 25.649 33.535 58.754 1.00 22.52 DIC ATOM 485 CB PRO 66 25.280 34.359 57.519 1.00 23.12 DIC ATOM 486 CG PRO 66 25.471 33.391 56.392 1.00 22.95 DIC ATOM 487 C PRO 66 24.440 32.880 59.421 1.00 21.35 DIC ATOM 488 O PRO 66 23.817 33.467 60.306 1.00 20.47 DIC ATOM 489 N ALA 67 24.124 31.657 59.009 1.00 20.26 DIC ATOM 490 CA ALA 67 22.992 30.937 59.577 1.00 20.00 DIC ATOM 491 CB ALA 67 22.771 29.619 58.823 1.00 21.70 DIC ATOM 492 C ALA 67 23.180 30.662 61.069 1.00 20.28 DIC ATOM 493 O ALA 67 22.202 30.487 61.797 1.00 19.39 DIC ATOM 494 N ASP 68 24.430 30.624 61.527 1.00 18.25 DIC ATOM 495 CA ASP 68 24.702 30.366 62.937 1.00 17.98 DIC ATOM 496 CB ASP 68 26.196 30.512 63.249 1.00 18.00 DIC ATOM 497 CG ASP 68 27.037 29.385 62.680 1.00 19.22 DIC ATOM 498 OD1 ASP 68 28.264 29.391 62.924 1.00 20.73 DIC ATOM 499 OD2 ASP 68 26.488 28.500 61.994 1.00 21.66 DIC ATOM 500 C ASP 68 23.941 31.323 63.853 1.00 17.42 DIC ATOM 501 O ASP 68 23.596 30.971 64.981 1.00 16.39 DIC ATOM 502 N PHE 69 23.679 32.531 63.371 1.00 16.56 DIC ATOM 503 CA PHE 69 23.005 33.527 64.192 1.00 18.20 DIC ATOM 504 CB PHE 69 23.823 34.821 64.160 1.00 18.04 DIC ATOM 505 CG PHE 69 25.314 34.583 64.118 1.00 18.37 DIC ATOM 506 CD1 PHE 69 25.983 34.473 62.898 1.00 18.98 DIC ATOM 507 CD2 PHE 69 26.039 34.431 65.293 1.00 16.47 DIC ATOM 508 CE1 PHE 69 27.354 34.215 62.852 1.00 18.40 DIC ATOM 509 CE2 PHE 69 27.410 34.172 65.264 1.00 16.90 DIC ATOM 510 CZ PHE 69 28.071 34.063 64.039 1.00 18.55 DIC ATOM 511 C PHE 69 21.565 33.796 63.778 1.00 20.05 DIC ATOM 512 O PHE 69 20.965 34.796 64.181 1.00 19.59 DIC ATOM 513 N ALA 70 21.004 32.884 62.995 1.00 21.70 DIC ATOM 514 CA ALA 70 19.638 33.030 62.509 1.00 23.13 DIC ATOM 515 CB ALA 70 19.253 31.812 61.678 1.00 24.32 DIC ATOM 516 C ALA 70 18.597 33.257 63.603 1.00 24.21 DIC ATOM 517 O ALA 70 17.553 33.857 63.348 1.00 25.81 DIC ATOM 518 N GLY 71 18.867 32.782 64.814 1.00 23.19 DIC ATOM 519 CA GLY 71 17.901 32.964 65.883 1.00 23.35 DIC ATOM 520 C GLY 71 17.929 34.315 66.583 1.00 22.92 DIC ATOM 521 O GLY 71 17.009 34.642 67.338 1.00 21.65 DIC ATOM 522 N PHE 72 18.966 35.109 66.331 1.00 21.05 DIC ATOM 523 CA PHE 72 19.105 36.415 66.976 1.00 20.69 DIC ATOM 524 CB PHE 72 20.592 36.786 67.069 1.00 20.82 DIC ATOM 525 CG PHE 72 21.414 35.823 67.901 1.00 22.40 DIC ATOM 526 CD1 PHE 72 22.787 36.003 68.041 1.00 21.53 DIC ATOM 527 CD2 PHE 72 20.817 34.737 68.540 1.00 22.26 DIC ATOM 528 CE1 PHE 72 23.554 35.116 68.803 1.00 23.86 DIC ATOM 529 CE2 PHE 72 21.573 33.843 69.305 1.00 23.97 DIC ATOM 530 CZ PHE 72 22.946 34.033 69.437 1.00 23.46 DIC ATOM 531 C PHE 72 18.316 37.539 66.296 1.00 20.09 DIC ATOM 532 O PHE 72 18.196 37.579 65.074 1.00 21.80 DIC ATOM 533 N PRO 73 17.783 38.480 67.090 1.00 19.37 DIC ATOM 534 CD PRO 73 18.031 38.670 68.529 1.00 19.40 DIC ATOM 535 CA PRO 73 17.002 39.599 66.558 1.00 18.84 DIC ATOM 536 CB PRO 73 16.675 40.418 67.807 1.00 19.67 DIC ATOM 537 CG PRO 73 17.826 40.159 68.687 1.00 19.66 DIC ATOM 538 C PRO 73 17.711 40.418 65.495 1.00 18.90 DIC ATOM 539 O PRO 73 18.905 40.705 65.596 1.00 16.76 DIC ATOM 540 N LEU 74 16.956 40.790 64.470 1.00 18.84 DIC ATOM 541 CA LEU 74 17.493 41.583 63.378 1.00 21.06 DIC ATOM 542 CB LEU 74 17.769 40.673 62.176 1.00 22.16 DIC ATOM 543 CG LEU 74 18.916 41.043 61.231 1.00 22.74 DIC ATOM 544 CD1 LEU 74 20.240 41.080 61.989 1.00 23.10 DIC ATOM 545 CD2 LEU 74 18.983 40.026 60.114 1.00 23.73 DIC ATOM 546 C LEU 74 16.438 42.637 63.040 1.00 21.30 DIC ATOM 547 O LEU 74 15.758 42.540 62.021 1.00 22.75 DIC ATOM 548 N ASN 75 16.308 43.634 63.915 1.00 21.53 DIC ATOM 549 CA ASN 75 15.329 44.708 63.749 1.00 20.41 DIC ATOM 550 CB ASN 75 14.716 45.101 65.125 1.00 22.53 DIC ATOM 551 CG ASN 75 15.767 45.292 66.259 1.00 25.80 DIC ATOM 552 OD1 ASN 75 16.458 44.349 66.665 1.00 23.29 DIC ATOM 553 ND2 ASN 75 15.854 46.520 66.791 1.00 26.49 DIC ATOM 554 C ASN 75 15.822 45.968 63.012 1.00 20.20 DIC ATOM 555 O ASN 75 15.036 46.654 62.355 1.00 18.24 DIC ATOM 556 N ILE 76 17.116 46.265 63.111 1.00 16.30 DIC ATOM 557 CA ILE 76 17.676 47.450 62.467 1.00 14.30 DIC ATOM 558 CB ILE 76 18.998 47.836 63.155 1.00 15.53 DIC ATOM 559 CG2 ILE 76 19.496 49.183 62.643 1.00 14.83 DIC ATOM 560 CG1 ILE 76 18.753 47.925 64.668 1.00 15.63 DIC ATOM 561 CD ILE 76 20.000 48.191 65.496 1.00 16.08 DIC ATOM 562 C ILE 76 17.869 47.172 60.976 1.00 13.06 DIC ATOM 563 O ILE 76 18.732 46.398 60.578 1.00 11.46 DIC ATOM 564 N ARG 77 17.036 47.813 60.161 1.00 12.41 DIC ATOM 565 CA ARG 77 17.033 47.606 58.719 1.00 11.27 DIC ATOM 566 CB ARG 77 16.016 48.544 58.071 1.00 11.91 DIC ATOM 567 CG ARG 77 15.774 48.285 56.589 1.00 14.32 DIC ATOM 568 CD ARG 77 14.766 49.291 56.023 1.00 17.97 DIC ATOM 569 NE ARG 77 14.418 48.999 54.637 1.00 19.40 DIC ATOM 570 CZ ARG 77 14.017 49.909 53.755 1.00 20.80 DIC ATOM 571 NH1 ARG 77 13.910 51.182 54.108 1.00 20.49 DIC ATOM 572 NH2 ARG 77 13.730 49.543 52.512 1.00 20.14 DIC ATOM 573 C ARG 77 18.363 47.718 57.980 1.00 10.68 DIC ATOM 574 O ARG 77 18.642 46.905 57.102 1.00 9.93 DIC ATOM 575 N HIS 78 19.184 48.709 58.318 1.00 9.86 DIC ATOM 576 CA HIS 78 20.455 48.876 57.613 1.00 11.66 DIC ATOM 577 CB HIS 78 20.975 50.316 57.782 1.00 12.15 DIC ATOM 578 CG HIS 78 21.469 50.635 59.160 1.00 11.23 DIC ATOM 579 CD2 HIS 78 20.830 51.149 60.238 1.00 9.90 DIC ATOM 580 ND1 HIS 78 22.779 50.447 59.545 1.00 14.19 DIC ATOM 581 CE1 HIS 78 22.927 50.834 60.801 1.00 11.70 DIC ATOM 582 NE2 HIS 78 21.758 51.264 61.244 1.00 13.16 DIC ATOM 583 C HIS 78 21.537 47.879 58.022 1.00 11.09 DIC ATOM 584 O HIS 78 22.637 47.898 57.474 1.00 10.55 DIC ATOM 585 N ILE 79 21.219 46.989 58.961 1.00 9.64 DIC ATOM 586 CA ILE 79 22.199 46.016 59.438 1.00 8.79 DIC ATOM 587 CB ILE 79 22.327 46.110 60.980 1.00 8.64 DIC ATOM 588 CG2 ILE 79 23.316 45.068 61.493 1.00 7.07 DIC ATOM 589 CG1 ILE 79 22.762 47.529 61.374 1.00 8.17 DIC ATOM 590 CD ILE 79 22.723 47.807 62.875 1.00 9.48 DIC ATOM 591 C ILE 79 21.874 44.568 59.053 1.00 10.57 DIC ATOM 592 O ILE 79 20.769 44.088 59.298 1.00 10.81 DIC ATOM 593 N SER 80 22.838 43.871 58.453 1.00 11.32 DIC ATOM 594 CA SER 80 22.632 42.473 58.065 1.00 10.85 DIC ATOM 595 CB SER 80 23.416 42.135 56.800 1.00 11.37 DIC ATOM 596 OG SER 80 24.804 42.239 57.045 1.00 11.89 DIC ATOM 597 C SER 80 23.098 41.556 59.193 1.00 11.08 DIC ATOM 598 O SER 80 23.788 41.999 60.117 1.00 11.39 DIC ATOM 599 N ILE 81 22.722 40.281 59.094 1.00 10.23 DIC ATOM 600 CA ILE 81 23.038 39.251 60.087 1.00 12.43 DIC ATOM 601 CB ILE 81 22.449 37.868 59.640 1.00 13.92 DIC ATOM 602 CG2 ILE 81 23.114 37.404 58.354 1.00 14.49 DIC ATOM 603 CG1 ILE 81 22.637 36.816 60.738 1.00 16.79 DIC ATOM 604 CD ILE 81 21.858 37.101 62.008 1.00 21.00 DIC ATOM 605 C ILE 81 24.533 39.113 60.388 1.00 11.38 DIC ATOM 606 O ILE 81 24.921 38.716 61.483 1.00 11.02 DIC ATOM 607 N THR 82 25.368 39.460 59.421 1.00 11.66 DIC ATOM 608 CA THR 82 26.816 39.382 59.590 1.00 13.55 DIC ATOM 609 CB THR 82 27.525 39.881 58.309 1.00 12.95 DIC ATOM 610 OG1 THR 82 27.238 38.981 57.235 1.00 15.78 DIC ATOM 611 OG2 THR 82 29.027 39.953 58.505 1.00 13.95 DIC ATOM 612 C THR 82 27.305 40.193 60.801 1.00 13.04 DIC ATOM 613 O THR 82 28.423 40.001 61.283 1.00 14.43 DIC ATOM 614 N THR 83 26.468 41.100 61.293 1.00 12.94 DIC ATOM 615 CA THR 83 26.843 41.925 62.444 1.00 10.16 DIC ATOM 616 CB THR 83 25.762 42.993 62.736 1.00 8.84 DIC ATOM 617 OG1 THR 83 26.255 43.900 63.729 1.00 8.21 DIC ATOM 618 CG2 THR 83 24.473 42.345 63.242 1.00 7.30 DIC ATOM 619 C THR 83 27.079 41.088 63.712 1.00 9.87 DIC ATOM 620 O THR 83 27.744 41.536 64.654 1.00 8.73 DIC ATOM 621 N TYR 84 26.545 39.869 63.732 1.00 8.10 DIC ATOM 622 CA TYR 84 26.719 38.990 64.889 1.00 9.50 DIC ATOM 623 CB TYR 84 25.508 38.073 65.061 1.00 8.94 DIC ATOM 624 CG TYR 84 24.278 38.731 65.627 1.00 10.26 DIC ATOM 625 CD1 TYR 84 23.194 39.044 64.805 1.00 10.22 DIC ATOM 626 CE1 TYR 84 22.036 39.613 65.327 1.00 10.08 DIC ATOM 627 CD2 TYR 84 24.179 39.011 66.994 1.00 10.47 DIC ATOM 628 CE2 TYR 84 23.028 39.581 67.527 1.00 9.14 DIC ATOM 629 CZ TYR 84 21.959 39.875 66.685 1.00 10.95 DIC ATOM 630 OH TYR 84 20.806 40.406 67.205 1.00 13.06 DIC ATOM 631 C TYR 84 27.965 38.104 64.835 1.00 9.18 DIC ATOM 632 O TYR 84 28.314 37.471 65.832 1.00 10.15 DIC ATOM 633 N ALA 85 28.641 38.054 63.689 1.00 9.06 DIC ATOM 634 CA ALA 85 29.814 37.185 63.554 1.00 8.72 DIC ATOM 635 CB ALA 85 30.394 37.294 62.145 1.00 9.77 DIC ATOM 636 C ALA 85 30.912 37.423 64.581 1.00 9.19 DIC ATOM 637 O ALA 85 31.599 36.486 64.993 1.00 8.82 DIC ATOM 638 N ARG 86 31.074 38.669 65.003 1.00 9.47 DIC ATOM 639 CA ARG 86 32.111 39.003 65.966 1.00 9.96 DIC ATOM 640 CB ARG 86 32.051 40.502 66.294 1.00 9.71 DIC ATOM 641 CG ARG 86 30.811 40.949 67.048 1.00 9.90 DIC ATOM 642 CD ARG 86 30.656 42.466 67.001 1.00 8.17 DIC ATOM 643 NE ARG 86 29.919 42.902 65.815 1.00 7.34 DIC ATOM 644 CZ ARG 86 29.791 44.169 65.430 1.00 8.06 DIC ATOM 645 NH1 ARG 86 30.357 45.142 66.133 1.00 6.00 DIC ATOM 646 NH2 ARG 86 29.079 44.464 64.347 1.00 8.41 DIC ATOM 647 C ARG 86 32.016 38.165 67.243 1.00 9.15 DIC ATOM 648 O ARG 86 33.030 37.911 67.896 1.00 9.85 DIC ATOM 649 N LEU 87 30.809 37.724 67.593 1.00 10.06 DIC ATOM 650 CA LEU 87 30.607 36.909 68.799 1.00 10.59 DIC ATOM 651 CB LEU 87 29.124 36.563 68.957 1.00 11.67 DIC ATOM 652 CG LEU 87 28.147 37.736 69.102 1.00 12.74 DIC ATOM 653 CD1 LEU 87 26.726 37.198 69.137 1.00 13.49 DIC ATOM 654 CD2 LEU 87 28.456 38.527 70.368 1.00 11.69 DIC ATOM 655 C LEU 87 31.435 35.613 68.832 1.00 11.32 DIC ATOM 656 O LEU 87 31.747 35.096 69.907 1.00 9.34 DIC ATOM 657 N LYS 88 31.781 35.085 67.658 1.00 12.29 DIC ATOM 658 CA LYS 88 32.575 33.849 67.575 1.00 12.77 DIC ATOM 659 CB LYS 88 31.995 32.914 66.506 1.00 13.12 DIC ATOM 660 CG LYS 88 30.724 32.181 66.926 1.00 14.09 DIC ATOM 661 CD LYS 88 30.390 31.098 65.907 1.00 14.18 DIC ATOM 662 CE LYS 88 29.287 30.182 66.387 1.00 16.96 DIC ATOM 663 NZ LYS 88 29.049 29.101 65.386 1.00 15.57 DIC ATOM 664 C LYS 88 34.043 34.120 67.252 1.00 12.47 DIC ATOM 665 O LYS 88 34.755 33.247 66.754 1.00 13.10 DIC ATOM 666 N LEU 89 34.495 35.332 67.540 1.00 11.63 DIC ATOM 667 CA LEU 89 35.874 35.710 67.263 1.00 13.26 DIC ATOM 668 CB LEU 89 36.117 37.141 67.760 1.00 14.71 DIC ATOM 669 CG LEU 89 36.901 38.093 66.853 1.00 18.28 DIC ATOM 670 CD1 LEU 89 36.517 37.918 65.401 1.00 18.01 DIC ATOM 671 CD2 LEU 89 36.632 39.520 67.302 1.00 19.23 DIC ATOM 672 C LEU 89 36.854 34.725 67.906 1.00 13.22 DIC ATOM 673 O LEU 89 37.878 34.378 67.314 1.00 14.28 DIC ATOM 674 N GLY 90 36.528 34.262 69.109 1.00 12.35 DIC ATOM 675 CA GLY 90 37.381 33.310 69.797 1.00 12.11 DIC ATOM 676 C GLY 90 37.553 32.001 69.041 1.00 14.28 DIC ATOM 677 O GLY 90 38.561 31.310 69.213 1.00 12.59 DIC ATOM 678 N GLU 91 36.577 31.667 68.197 1.00 14.29 DIC ATOM 679 CA GLU 91 36.612 30.440 67.395 1.00 15.06 DIC ATOM 680 CB GLU 91 35.194 29.912 67.159 1.00 16.79 DIC ATOM 681 CG GLU 91 34.447 29.384 68.383 1.00 19.76 DIC ATOM 682 CD GLU 91 33.104 28.774 67.992 1.00 23.18 DIC ATOM 683 OE1 GLU 91 33.086 27.933 67.064 1.00 22.19 DIC ATOM 684 OE2 GLU 91 32.071 29.132 68.606 1.00 23.20 DIC ATOM 685 C GLU 91 37.259 30.635 66.016 1.00 14.78 DIC ATOM 686 O GLU 91 37.855 29.705 65.465 1.00 14.56 DIC ATOM 687 N TYR 92 37.119 31.839 65.467 1.00 14.84 DIC ATOM 688 CA TYR 92 37.636 32.175 64.140 1.00 16.06 DIC ATOM 689 CB TYR 92 36.850 33.354 63.549 1.00 14.49 DIC ATOM 690 CG TYR 92 35.356 33.128 63.399 1.00 15.73 DIC ATOM 691 CD1 TYR 92 34.856 31.930 62.889 1.00 15.13 DIC ATOM 692 CE1 TYR 92 33.483 31.741 62.698 1.00 16.39 DIC ATOM 693 CD2 TYR 92 34.445 34.139 63.720 1.00 15.08 DIC ATOM 694 CE2 TYR 92 33.073 33.962 63.532 1.00 16.55 DIC ATOM 695 CZ TYR 92 32.601 32.762 63.019 1.00 15.33 DIC ATOM 696 OH TYR 92 31.254 32.591 62.813 1.00 15.89 DIC ATOM 697 C TYR 92 39.122 32.516 64.050 1.00 16.64 DIC ATOM 698 O TYR 92 39.749 32.286 63.025 1.00 18.19 DIC ATOM 699 N ILE 93 39.680 33.084 65.109 1.00 18.45 DIC ATOM 700 CA ILE 93 41.085 33.468 65.089 1.00 19.66 DIC ATOM 701 CB ILE 93 41.221 35.001 65.239 1.00 20.11 DIC ATOM 702 CG2 ILE 93 42.690 35.389 65.380 1.00 18.82 DIC ATOM 703 CG1 ILE 93 40.562 35.684 64.031 1.00 19.68 DIC ATOM 704 CD ILE 93 40.589 37.195 64.072 1.00 20.89 DIC ATOM 705 C ILE 93 41.880 32.761 66.175 1.00 20.25 DIC ATOM 706 O ILE 93 41.553 32.845 67.361 1.00 19.56 DIC ATOM 707 N ALA 94 42.934 32.070 65.763 1.00 20.40 DIC ATOM 708 CA ALA 94 43.753 31.323 66.705 1.00 23.20 DIC ATOM 709 CB ALA 94 43.888 29.890 66.226 1.00 23.20 DIC ATOM 710 C ALA 94 45.136 31.923 66.921 1.00 24.59 DIC ATOM 711 O ALA 94 45.707 31.804 68.009 1.00 24.30 DIC ATOM 712 N ASP 95 45.660 32.574 65.888 1.00 26.69 DIC ATOM 713 CA ASP 95 46.995 33.163 65.930 1.00 29.50 DIC ATOM 714 CB ASP 95 47.572 33.219 64.509 1.00 31.58 DIC ATOM 715 CG ASP 95 46.640 33.908 63.524 1.00 35.84 DIC ATOM 716 OD1 ASP 95 47.039 34.104 62.355 1.00 38.60 DIC ATOM 717 OD2 ASP 95 45.504 34.252 63.913 1.00 38.61 DIC ATOM 718 C ASP 95 47.147 34.542 66.580 1.00 29.37 DIC ATOM 719 O ASP 95 48.141 35.224 66.333 1.00 31.82 DIC ATOM 720 N GYS 96 46.193 34.958 67.408 1.00 26.90 DIC ATOM 721 CA GYS 96 46.298 36.268 68.052 1.00 25.49 DIC ATOM 722 CB GYS 96 45.516 37.325 67.260 1.00 25.52 DIC ATOM 723 SG GYS 96 46.072 37.567 65.572 1.00 24.86 DIC ATOM 724 C GYS 96 45.793 36.288 69.484 1.00 24.23 DIC ATOM 725 O GYS 96 44.733 35.738 69.785 1.00 25.00 DIC ATOM 726 N ASP 97 46.549 36.927 70.368 1.00 22.41 DIC ATOM 727 CA ASP 97 46.122 37.044 71.756 1.00 22.45 DIC ATOM 728 CB ASP 97 47.326 37.111 72.689 1.00 22.93 DIC ATOM 729 CG ASP 97 47.968 35.760 72.901 1.00 24.22 DIC ATOM 730 OD1 ASP 97 49.053 35.713 73.516 1.00 26.27 DIC ATOM 731 OD2 ASP 97 47.384 34.748 72.457 1.00 25.38 DIC ATOM 732 C ASP 97 45.297 38.317 71.891 1.00 21.90 DIC ATOM 733 O ASP 97 44.517 38.471 72.830 1.00 23.11 DIC ATOM 734 N LYS 98 45.473 39.226 70.939 1.00 19.23 DIC ATOM 735 CA LYS 98 44.749 40.494 70.948 1.00 18.34 DIC ATOM 736 CB LYS 98 45.573 41.576 71.657 1.00 20.35 DIC ATOM 737 CG LYS 98 44.979 42.983 71.560 1.00 22.09 DIC ATOM 738 CD LYS 98 45.971 44.075 71.993 1.00 22.26 DIC ATOM 739 CE LYS 98 46.314 43.997 73.472 1.00 22.69 DIC ATOM 740 NZ LYS 98 46.981 45.238 73.980 1.00 20.82 DIC ATOM 741 C LYS 98 44.471 40.933 69.519 1.00 16.18 DIC ATOM 742 O LYS 98 45.324 40.795 68.642 1.00 13.58 DIC ATOM 743 N VAL 99 43.264 41.434 69.284 1.00 14.00 DIC ATOM 744 CA VAL 99 42.891 41.917 67.963 1.00 13.34 DIC ATOM 745 CB VAL 99 42.064 40.881 67.170 1.00 12.63 DIC ATOM 746 CG1 VAL 99 42.891 39.626 66.923 1.00 11.07 DIC ATOM 747 CG2 VAL 99 40.782 40.546 67.922 1.00 13.64 DIC ATOM 748 C VAL 99 42.058 43.169 68.141 1.00 13.18 DIC ATOM 749 O VAL 99 41.428 43.361 69.180 1.00 12.75 DIC ATOM 750 N LEU 100 42.081 44.033 67.136 1.00 11.89 DIC ATOM 751 CA LEU 100 41.304 45.257 67.181 1.00 12.48 DIC ATOM 752 CB LEU 100 42.183 46.473 66.870 1.00 13.07 DIC ATOM 753 CG LEU 100 41.498 47.849 66.824 1.00 16.10 DIC ATOM 754 CD1 LEU 100 40.525 47.996 67.984 1.00 15.54 DIC ATOM 755 CD2 LEU 100 42.558 48.940 66.881 1.00 15.51 DIC ATOM 756 C LEU 100 40.200 45.122 66.153 1.00 12.39 DIC ATOM 757 O LEU 100 40.458 45.100 64.941 1.00 12.90 DIC ATOM 758 N TYR 101 38.972 45.014 66.651 1.00 11.19 DIC ATOM 759 CA TYR 101 37.802 44.862 65.804 1.00 11.19 DIC ATOM 760 CB TYR 101 36.703 44.095 66.539 1.00 13.00 DIC ATOM 761 CG TYR 101 35.517 43.788 65.652 1.00 15.87 DIC ATOM 762 CD1 TYR 101 35.497 42.628 64.881 1.00 18.26 DIC ATOM 763 CE1 TYR 101 34.440 42.343 64.035 1.00 21.70 DIC ATOM 764 CD2 TYR 101 34.438 44.667 65.549 1.00 18.95 DIC ATOM 765 CE2 TYR 101 33.360 44.389 64.690 1.00 21.15 DIC ATOM 766 CZ TYR 101 33.376 43.219 63.942 1.00 21.56 DIC ATOM 767 OH TYR 101 32.328 42.882 63.115 1.00 26.24 DIC ATOM 768 C TYR 101 37.236 46.214 65.392 1.00 10.61 DIC ATOM 769 O TYR 101 37.076 47.108 66.228 1.00 9.84 DIC ATOM 770 N LEU 102 36.922 46.354 64.108 1.00 9.31 DIC ATOM 771 CA LEU 102 36.345 47.588 63.601 1.00 9.32 DIC ATOM 772 CB LEU 102 37.359 48.365 62.762 1.00 10.13 DIC ATOM 773 CG LEU 102 38.698 48.757 63.390 1.00 11.91 DIC ATOM 774 CD1 LEU 102 39.612 49.271 62.304 1.00 8.61 DIC ATOM 775 CD2 LEU 102 38.488 49.797 64.484 1.00 9.84 DIC ATOM 776 C LEU 102 35.135 47.298 62.725 1.00 9.76 DIC ATOM 777 O LEU 102 35.123 46.319 61.970 1.00 10.61 DIC ATOM 778 N ASP 103 34.119 48.149 62.834 1.00 8.81 DIC ATOM 779 CA ASP 103 32.938 48.028 61.993 1.00 10.01 DIC ATOM 780 CB ASP 103 31.848 48.969 62.449 1.00 8.25 DIC ATOM 781 CG ASP 103 30.891 48.371 63.428 1.00 9.78 DIC ATOM 782 OD1 ASP 103 29.964 49.092 63.841 1.00 8.38 DIC ATOM 783 OD2 ASP 103 31.050 47.196 63.787 1.00 8.21 DIC ATOM 784 C ASP 103 33.408 48.465 60.607 1.00 9.24 DIC ATOM 785 O ASP 103 34.485 49.041 60.463 1.00 7.13 DIC ATOM 786 N ILE 104 32.591 48.218 59.594 1.00 11.58 DIC ATOM 787 CA ILE 104 32.946 48.594 58.226 1.00 10.90 DIC ATOM 788 CB ILE 104 32.103 47.800 57.203 1.00 11.09 DIC ATOM 789 CG2 ILE 104 32.432 48.255 55.785 1.00 10.13 DIC ATOM 790 CG1 ILE 104 32.361 46.295 57.365 1.00 9.33 DIC ATOM 791 CD ILE 104 33.764 45.856 57.023 1.00 8.77 DIC ATOM 792 C ILE 104 32.732 50.085 57.980 1.00 11.23 DIC ATOM 793 O ILE 104 33.430 50.691 57.164 1.00 10.66 DIC ATOM 794 N ASP 105 31.764 50.667 58.687 1.00 10.09 DIC ATOM 795 CA ASP 105 31.439 52.085 58.545 1.00 10.37 DIC ATOM 796 CB ASP 105 29.959 52.325 58.896 1.00 9.81 DIC ATOM 797 CG ASP 105 29.608 51.900 60.318 1.00 7.95 DIC ATOM 798 OD1 ASP 105 30.413 51.181 60.955 1.00 10.48 DIC ATOM 799 OD2 ASP 105 28.510 52.275 60.799 1.00 8.90 DIC ATOM 800 C ASP 105 32.328 52.996 59.397 1.00 11.29 DIC ATOM 801 O ASP 105 31.838 53.871 60.121 1.00 10.81 DIC ATOM 802 N VAL 106 33.637 52.774 59.323 1.00 12.07 DIC ATOM 803 CA VAL 106 34.582 53.600 60.061 1.00 12.81 DIC ATOM 804 CB VAL 106 35.307 52.818 61.191 1.00 14.09 DIC ATOM 805 CG1 VAL 106 34.290 52.149 62.097 1.00 9.82 DIC ATOM 806 CG2 VAL 106 36.278 51.805 60.588 1.00 13.66 DIC ATOM 807 C VAL 106 35.641 54.127 59.106 1.00 13.02 DIC ATOM 808 O VAL 106 35.901 53.545 58.050 1.00 12.85 DIC ATOM 809 N LEU 107 36.241 55.242 59.490 1.00 14.12 DIC ATOM 810 CA LEU 107 37.288 55.875 58.710 1.00 14.17 DIC ATOM 811 CB LEU 107 36.743 57.141 58.050 1.00 15.58 DIC ATOM 812 CG LEU 107 36.665 57.238 56.522 1.00 18.69 DIC ATOM 813 CD1 LEU 107 36.107 55.963 55.914 1.00 19.47 DIC ATOM 814 CD2 LEU 107 35.800 58.438 56.155 1.00 18.85 DIC ATOM 815 C LEU 107 38.364 56.220 59.734 1.00 13.89 DIC ATOM 816 O LEU 107 38.165 57.089 60.581 1.00 13.18 DIC ATOM 817 N VAL 108 39.485 55.511 59.686 1.00 14.30 DIC ATOM 818 CA VAL 106 40.575 55.766 60.625 1.00 14.74 DIC ATOM 819 CB VAL 108 41.566 54.581 60.654 1.00 14.99 DIC ATOM 820 CG1 VAL 108 42.703 54.861 61.648 1.00 12.98 DIC ATOM 821 CG2 VAL 108 40.825 53.316 61.039 1.00 14.00 DIC ATOM 822 C VAL 108 41.281 57.027 60.159 1.00 15.87 DIC ATOM 823 O VAL 108 41.740 57.093 59.015 1.00 17.65 DIC ATOM 824 N ARG 109 41.350 58.034 61.029 1.00 17.02 DIC ATOM 825 CA ARG 109 41.981 59.305 60.668 1.00 17.83 DIC ATOM 826 CB ARG 109 41.011 60.467 60.903 1.00 20.81 DIC ATOM 827 CG ARG 109 39.553 60.066 60.959 1.00 25.33 DIC ATOM 828 CD ARG 109 38.684 61.042 60.198 1.00 27.87 DIC ATOM 829 NE ARG 109 39.003 62.443 60.463 1.00 30.93 DIC ATOM 830 CZ ARG 109 38.574 63.450 59.702 1.00 31.43 DIC ATOM 831 NH1 ARG 109 38.902 64.702 59.994 1.00 29.96 DIC ATOM 832 NH2 ARG 109 37.817 63.198 58.640 1.00 29.66 DIC ATOM 833 C ARG 109 43.277 59.603 61.413 1.00 18.31 DIC ATOM 834 O ARG 109 43.945 60.597 61.127 1.00 18.37 DIC ATOM 835 N ASP 110 43.614 58.767 62.388 1.00 15.42 DIC ATOM 836 CA ASP 110 44.846 58.952 63.143 1.00 16.34 DIC ATOM 837 CB ASP 110 44.627 59.926 64.312 1.00 18.08 DIC ATOM 838 CG ASP 110 45.936 60.528 64.830 1.00 22.13 DIC ATOM 839 OD1 ASP 110 46.857 60.743 64.015 1.00 21.78 DIC ATOM 840 OD2 ASP 110 46.040 60.802 66.045 1.00 23.13 DIC ATOM 841 C ASP 110 45.303 57.590 63.653 1.00 14.85 DIC ATOM 842 O ASP 110 44.523 56.645 63.698 1.00 13.20 DIC ATOM 843 N ARG 111 46.571 57.499 64.028 1.00 15.06 DIC ATOM 844 CA ARG 111 47.146 56.255 64.510 1.00 15.16 DIC ATOM 845 CB ARG 111 48.553 56.524 65.030 1.00 18.81 DIC ATOM 846 CG ARG 111 49.217 55.331 65.622 1.00 18.92 DIC ATOM 847 CD ARG 111 49.846 55.728 66.938 1.00 31.56 DIC ATOM 848 NE ARG 111 50.989 56.627 66.821 1.00 33.85 DIC ATOM 849 CZ ARG 111 51.668 57.080 67.869 1.00 36.04 DIC ATOM 850 NH1 ARG 111 51.307 56.709 69.092 1.00 34.31 DIC ATOM 851 NH2 ARG 111 52.706 57.897 67.699 1.00 37.36 DIC ATOM 852 C ARG 111 46.315 55.573 65.596 1.00 13.47 DIC ATOM 853 O ARG 111 45.751 56.226 66.473 1.00 10.45 DIC ATOM 854 N LEU 112 46.268 54.248 65.534 1.00 11.22 DIC ATOM 855 CA LEU 112 45.520 53.445 66.493 1.00 12.34 DIC ATOM 856 CB LEU 112 44.797 52.318 65.747 1.00 13.02 DIC ATOM 857 CG LEU 112 43.282 52.409 65.491 1.00 17.78 DIC ATOM 858 CD1 LEU 112 42.810 53.847 65.418 1.00 15.27 DIC ATOM 859 CD2 LEU 112 42.951 51.643 64.218 1.00 14.01 DIC ATOM 860 C LEU 112 46.455 52.853 67.545 1.00 11.08 DIC ATOM 861 O LEU 112 46.013 52.187 68.481 1.00 10.55 DIC ATOM 862 N THR 113 47.749 53.105 67.397 1.00 10.99 DIC ATOM 863 CA THR 113 48.735 52.555 68.322 1.00 13.17 DIC ATOM 864 CB THR 113 50.146 53.084 67.987 1.00 14.67 DIC ATOM 865 OG1 THR 113 50.429 52.810 66.607 1.00 15.24 DIC ATOM 866 CG2 THR 113 51.203 52.421 68.863 1.00 14.83 DIC ATOM 867 C THR 113 48.423 52.788 69.802 1.00 13.22 DIC ATOM 868 O THR 113 48.550 51.869 70.616 1.00 13.60 DIC ATOM 869 N PRO 114 48.009 54.013 70.177 1.00 13.02 DIC ATOM 870 CD PRO 114 47.875 55.254 69.398 1.00 12.48 DIC ATOM 871 CA PRO 114 47.701 54.250 71.593 1.00 13.64 DIC ATOM 872 CB PRO 114 47.182 55.686 71.600 1.00 14.06 DIC ATOM 873 CG PRO 114 47.955 56.321 70.468 1.00 14.40 DIC ATOM 874 C PRO 114 46.651 53.268 72.098 1.00 12.02 DIC ATOM 875 O PRO 114 46.751 52.759 73.211 1.00 13.45 DIC ATOM 876 N LEU 115 45.643 53.003 71.272 1.00 11.75 DIC ATOM 877 CA LEU 115 44.582 52.076 71.659 1.00 11.54 DIC ATOM 878 CB LEU 115 43.389 52.193 70.696 1.00 10.01 DIC ATOM 879 CG LEU 115 42.236 51.214 70.936 1.00 11.01 DIC ATOM 880 CD1 LEU 115 41.718 51.381 72.358 1.00 10.94 DIC ATOM 881 CD2 LEU 115 41.116 51.460 69.921 1.00 11.28 DIC ATOM 882 C LEU 115 45.131 50.656 71.656 1.00 10.96 DIC ATOM 883 O LEU 115 44.949 49.905 72.613 1.00 12.79 DIC ATOM 884 N TRP 116 45.817 50.301 70.578 1.00 11.17 DIC ATOM 885 CA TRP 116 46.410 48.977 70.443 1.00 12.32 DIC ATOM 886 CB TRP 116 47.161 48.880 69.113 1.00 11.64 DIC ATOM 887 CG TRP 116 47.885 47.579 68.933 1.00 14.42 DIC ATOM 888 CD2 TRP 116 47.304 46.314 68.595 1.00 12.78 DIC ATOM 889 CE2 TRP 116 48.352 45.365 68.570 1.00 13.04 DIC ATOM 890 CE3 TRP 116 45.996 45.887 68.312 1.00 13.68 DIC ATOM 891 CD1 TRP 116 49.222 47.355 69.096 1.00 14.44 DIC ATOM 892 NE1 TRP 116 49.511 46.027 68.878 1.00 14.14 DIC ATOM 893 CZ2 TRP 116 48.137 44.014 68.272 1.00 12.47 DIC ATOM 894 CZ3 TRP 116 45.782 44.539 68.014 1.00 13.84 DIC ATOM 895 CH2 TRP 116 46.851 43.621 67.997 1.00 13.37 DIC ATOM 896 C TRP 116 47.356 48.645 71.599 1.00 12.95 DIC ATOM 897 O TRP 116 47.404 47.504 72.056 1.00 13.17 DIC ATOM 898 N ASP 117 48.092 49.641 72.082 1.00 14.18 DIC ATOM 899 CA ASP 117 49.038 49.416 73.173 1.00 13.65 DIC ATOM 900 CB ASP 117 50.122 50.502 73.180 1.00 12.84 DIC ATOM 901 CG ASP 117 51.066 50.395 71.998 1.00 15.20 DIC ATOM 902 OD1 ASP 117 51.218 49.285 71.446 1.00 11.63 DIC ATOM 903 OD2 ASP 117 51.668 51.423 71.631 1.00 16.23 DIC ATOM 904 C ASP 117 48.403 49.352 74.554 1.00 14.05 DIC ATOM 905 O ASP 117 49.089 49.088 75.546 1.00 13.05 DIC ATOM 906 N THR 118 47.099 49.593 74.624 1.00 14.89 DIC ATOM 907 CA THR 118 46.401 49.572 75.903 1.00 15.50 DIC ATOM 908 CB THR 118 44.935 50.017 75.736 1.00 16.17 DIC ATOM 909 OG1 THR 118 44.902 51.379 75.272 1.00 16.94 DIC ATOM 910 CG2 THR 118 44.197 49.922 77.066 1.00 16.68 DIC ATOM 911 C THR 118 46.440 48.189 76.542 1.00 16.76 DIC ATOM 912 O THR 118 46.188 47.181 75.885 1.00 16.13 DIC ATOM 913 N ASP 119 46.769 48.140 77.827 1.00 17.70 DIC ATOM 914 CA ASP 119 46.816 46.861 78.531 1.00 19.90 DIC ATOM 915 CB ASP 119 47.841 46.926 79.669 1.00 22.37 DIC ATOM 916 CG ASP 119 47.885 45.653 80.501 1.00 24.15 DIC ATOM 917 OD1 ASP 119 47.539 44.567 79.989 1.00 22.37 DIC ATOM 918 OD2 ASP 119 48.289 45.744 81.678 1.00 26.50 DIC ATOM 919 C ASP 119 45.422 46.543 79.066 1.00 19.45 DIC ATOM 920 O ASP 119 44.899 47.250 79.931 1.00 20.25 DIC ATOM 921 N LEU 120 44.823 45.484 78.528 1.00 19.08 DIC ATOM 922 CA LEU 120 43.480 45.051 78.916 1.00 19.39 DIC ATOM 923 CB LEU 120 42.906 44.117 77.846 1.00 16.25 DIC ATOM 924 CG LEU 120 42.192 44.700 76.623 1.00 18.43 DIC ATOM 925 CD1 LEU 120 42.797 46.005 76.207 1.00 19.56 DIC ATOM 926 CD2 LEU 120 42.246 43.680 75.502 1.00 14.56 DIC ATOM 927 C LEU 120 43.413 44.342 80.264 1.00 19.79 DIC ATOM 928 O LEU 120 42.337 44.230 80.852 1.00 21.22 DIC ATOM 929 N GLY 121 44.552 43.861 80.754 1.00 20.41 DIC ATOM 930 CA GLY 121 44.539 43.156 82.024 1.00 20.26 DIC ATOM 931 C GLY 121 43.648 41.934 81.880 1.00 20.32 DIC ATOM 932 O GLY 121 43.738 41.213 80.880 1.00 18.77 DIC ATOM 933 N ASN 122 42.778 41.695 82.855 1.00 20.30 DIC ATOM 934 CA ASN 122 41.891 40.540 82.772 1.00 21.26 DIC ATOM 935 CB ASN 122 41.778 39.852 84.135 1.00 23.94 DIC ATOM 936 CG ASN 122 41.067 38.510 84.054 1.00 27.72 DIC ATOM 937 OD1 ASN 122 41.427 37.643 83.247 1.00 29.43 DIC ATOM 938 ND2 ASN 122 40.056 38.329 84.893 1.00 29.68 DIC ATOM 939 C ASN 122 40.508 40.940 82.254 1.00 20.06 DIC ATOM 940 O ASN 122 39.545 40.173 82.356 1.00 19.14 DIC ATOM 941 N ASN 123 40.421 42.150 81.704 1.00 18.17 DIC ATOM 942 CA ASN 123 39.173 42.656 81.137 1.00 17.70 DIC ATOM 943 CB ASN 123 39.278 44.158 80.810 1.00 19.01 DIC ATOM 944 CG ASN 123 39.293 45.042 82.053 1.00 20.14 DIC ATOM 945 OD1 ASN 123 40.257 45.769 82.303 1.00 19.33 DIC ATOM 946 ND2 ASN 123 38.218 44.990 82.829 1.00 17.24 DIC ATOM 947 C ASN 123 38.894 41.891 79.842 1.00 17.42 DIC ATOM 948 O ASN 123 39.818 41.387 79.194 1.00 16.53 DIC ATOM 949 N TRP 124 37.619 41.823 79.469 1.00 16.21 DIC ATOM 950 CA TRP 124 37.191 41.136 78.260 1.00 13.67 DIC ATOM 951 CB TRP 124 35.675 40.980 78.246 1.00 13.09 DIC ATOM 952 CG TRP 124 35.140 40.061 79.278 1.00 14.06 DIC ATOM 953 CD2 TRP 124 35.114 38.631 79.212 1.00 13.39 DIC ATOM 954 CE2 TRP 124 34.475 38.169 80.389 1.00 14.28 DIC ATOM 955 CE3 TRP 124 35.566 37.694 78.273 1.00 14.36 DIC ATOM 956 CD1 TRP 124 34.535 40.406 80.461 1.00 11.88 DIC ATOM 957 NE1 TRP 124 34.131 39.272 81.132 1.00 12.38 DIC ATOM 958 CZ2 TRP 124 34.278 36.808 80.649 1.00 13.77 DIC ATOM 959 CZ3 TRP 124 35.370 36.338 78.534 1.00 15.53 DIC ATOM 960 CH2 TRP 124 34.730 35.911 79.714 1.00 15.41 DIC ATOM 961 C TRP 124 37.591 41.898 77.006 1.00 13.43 DIC ATOM 962 O TRP 124 37.899 41.303 75.979 1.00 12.54 DIC ATOM 963 N LEU 125 37.570 43.221 77.102 1.00 11.84 DIC ATOM 964 CA LEU 125 37.897 44.062 75.970 1.00 11.77 DIC ATOM 965 CB LEU 125 36.845 43.874 74.861 1.00 10.08 DIC ATOM 966 CG LEU 125 35.361 43.957 75.259 1.00 10.79 DIC ATOM 967 CD1 LEU 125 35.006 45.378 75.672 1.00 14.40 DIC ATOM 968 CD2 LEU 125 34.486 43.530 74.086 1.00 11.76 DIC ATOM 969 C LEU 125 37.958 45.524 76.368 1.00 11.36 DIC ATOM 970 O LEU 125 37.614 45.904 77.488 1.00 12.15 DIC ATOM 971 N GLY 126 38.419 46.336 75.432 1.00 11.25 DIC ATOM 972 CA GLY 126 38.492 47.763 75.651 1.00 11.38 DIC ATOM 973 C GLY 126 37.584 48.350 74.588 1.00 11.99 DIC ATOM 974 O GLY 126 37.600 47.893 73.435 1.00 11.61 DIC ATOM 975 N ALA 127 36.779 49.338 74.962 1.00 10.89 DIC ATOM 976 CA ALA 127 35.868 49.967 74.013 1.00 10.27 DIC ATOM 977 CB ALA 127 34.608 49.121 73.871 1.00 9.81 DIC ATOM 978 C ALA 127 35.499 51.383 74.444 1.00 11.20 DIC ATOM 979 O ALA 127 35.663 51.749 75.612 1.00 8.75 DIC ATOM 980 N SER 128 35.017 52.185 73.496 1.00 10.96 DIC ATOM 981 CA SER 128 34.622 53.551 73.811 1.00 12.41 DIC ATOM 982 CB SER 128 34.844 54.480 72.610 1.00 11.48 DIC ATOM 983 OG SER 128 36.228 54.600 72.303 1.00 12.36 DIC ATOM 984 C SER 128 33.153 53.563 74.220 1.00 13.04 DIC ATOM 985 O SER 128 32.362 52.717 73.783 1.00 11.02 DIC ATOM 986 N ILE 129 32.800 54.535 75.055 1.00 12.60 DIC ATOM 987 CA ILE 129 31.441 54.678 75.568 1.00 14.09 DIC ATOM 988 CB ILE 129 31.433 55.609 76.816 1.00 14.78 DIC ATOM 989 CG2 ILE 129 30.009 55.993 77.195 1.00 15.61 DIC ATOM 990 CG1 ILE 129 32.154 54.916 77.973 1.00 16.10 DIC ATOM 991 CD ILE 129 32.334 55.785 79.199 1.00 16.05 DIC ATOM 992 C ILE 129 30.484 55.232 74.519 1.00 14.40 DIC ATOM 993 O ILE 129 30.841 56.112 73.736 1.00 12.33 DIC ATOM 994 N ASP 130 29.263 54.708 74.513 1.00 14.40 DIC ATOM 995 CA ASP 130 28.253 55.155 73.571 1.00 14.93 DIC ATOM 996 CB ASP 130 27.396 53.972 73.127 1.00 13.65 DIC ATOM 997 CG ASP 130 26.533 54.305 71.936 1.00 12.84 DIC ATOM 998 OD1 ASP 130 25.787 55.315 71.985 1.00 15.16 DIC ATOM 999 OD2 ASP 130 26.605 53.556 70.953 1.00 12.26 DIC ATOM 1000 C ASP 130 27.359 56.209 74.228 1.00 14.81 DIC ATOM 1001 O ASP 130 26.458 55.868 74.991 1.00 15.34 DIC ATOM 1002 N LEU 131 27.605 57.482 73.932 1.00 15.23 DIC ATOM 1003 CA LEU 131 26.811 58.576 74.509 1.00 15.08 DIC ATOM 1004 CB LEU 131 27.344 59.936 74.049 1.00 15.03 DIC ATOM 1005 CG LEU 131 28.638 60.445 74.680 1.00 18.24 DIC ATOM 1006 CD1 LEU 131 29.710 59.364 74.623 1.00 20.00 DIC ATOM 1007 CD2 LEU 131 29.090 61.700 73.947 1.00 16.98 DIC ATOM 1008 C LEU 131 25.339 58.497 74.139 1.00 14.84 DIC ATOM 1009 O LEU 131 24.466 58.863 74.933 1.00 15.29 DIC ATOM 1010 N PHE 132 25.068 58.041 72.922 1.00 13.40 DIC ATOM 1011 CA PHE 132 23.700 57.930 72.440 1.00 15.19 DIC ATOM 1012 CB PHE 132 23.698 57.464 70.976 1.00 16.45 DIC ATOM 1013 CG PHE 132 22.325 57.299 70.391 1.00 18.23 DIC ATOM 1014 CD1 PHE 132 21.657 56.079 70.480 1.00 19.03 DIC ATOM 1015 CD2 PHE 132 21.680 58.371 69.793 1.00 19.73 DIC ATOM 1016 CE1 PHE 132 20.365 55.931 69.984 1.00 18.68 DIC ATOM 1017 CE2 PHE 132 20.381 58.235 69.292 1.00 21.22 DIC ATOM 1018 CZ PHE 132 19.723 57.010 69.389 1.00 19.92 DIC ATOM 1019 C PHE 132 22.898 56.971 73.320 1.00 15.39 DIC ATOM 1020 O PHE 132 21.812 57.316 73.791 1.00 17.07 DIC ATOM 1021 N VAL 133 23.446 55.781 73.553 1.00 12.91 DIC ATOM 1022 CA VAL 133 22.771 54.783 74.375 1.00 14.30 DIC ATOM 1023 CB VAL 133 23.439 53.399 74.241 1.00 13.72 DIC ATOM 1024 CG1 VAL 133 22.727 52.386 75.138 1.00 14.53 DIC ATOM 1025 CG2 VAL 133 23.375 52.939 72.794 1.00 13.31 DIC ATOM 1026 C VAL 133 22.741 55.184 75.845 1.00 15.10 DIC ATOM 1027 O VAL 133 21.710 55.049 76.503 1.00 15.38 DIC ATOM 1028 N GLU 134 23.867 55.682 76.352 1.00 16.89 DIC ATOM 1029 CA GLU 134 23.951 56.121 77.746 1.00 18.11 DIC ATOM 1030 CB GLU 134 25.334 56.708 78.058 1.00 17.79 DIC ATOM 1031 CG GLU 134 26.358 55.714 78.580 1.00 18.79 DIC ATOM 1032 CD GLU 134 25.943 55.071 79.893 1.00 15.84 DIC ATOM 1033 OE1 GLU 134 25.534 55.790 80.828 1.00 18.93 DIC ATOM 1034 OE2 GLU 134 26.035 53.838 79.993 1.00 16.91 DIC ATOM 1035 C GLU 134 22.904 57.169 78.092 1.00 18.74 DIC ATOM 1036 O GLU 134 22.397 57.196 79.207 1.00 19.62 DIC ATOM 1037 N ARG 135 22.583 58.054 77.163 1.00 20.18 DIC ATOM 1038 CA ARG 135 21.592 59.061 77.501 1.00 21.49 DIC ATOM 1039 CB ARG 135 21.898 60.402 76.820 1.00 22.17 DIC ATOM 1040 CG ARG 135 21.852 60.441 75.309 1.00 26.54 DIC ATOM 1041 CD ARG 135 22.447 61.769 74.834 1.00 30.72 DIC ATOM 1042 NE ARG 135 21.803 62.903 75.492 1.00 33.69 DIC ATOM 1043 CZ ARG 135 20.912 63.708 74.916 1.00 35.46 DIC ATOM 1044 NH1 ARG 135 20.380 64.705 75.612 1.00 36.28 DIC ATOM 1045 NH2 ARG 135 20.568 63.535 73.646 1.00 33.44 DIC ATOM 1046 C ARG 135 20.176 58.599 77.196 1.00 21.50 DIC ATOM 1047 O ARG 135 19.231 59.380 77.266 1.00 21.59 DIC ATOM 1048 N GLN 136 20.021 57.321 76.867 1.00 20.53 DIC ATOM 1049 CA GLN 136 18.689 56.790 76.600 1.00 21.69 DIC ATOM 1050 CB GLN 136 18.767 55.590 75.653 1.00 22.18 DIC ATOM 1051 CG GLN 136 17.408 55.118 75.147 1.00 24.69 DIC ATOM 1052 CD GLN 136 17.487 53.951 74.173 1.00 27.02 DIC ATOM 1053 OE1 GLN 136 18.419 53.858 73.384 1.00 26.51 DIC ATOM 1054 NE2 GLN 136 16.491 53.067 74.216 1.00 26.50 DIC ATOM 1055 C GLN 136 18.067 56.361 77.938 1.00 23.33 DIC ATOM 1056 O GLN 136 18.334 55.271 78.431 1.00 21.46 DIC ATOM 1057 N GLU 137 17.241 57.237 78.510 1.00 23.90 DIC ATOM 1058 CA GLU 137 16.549 57.028 79.789 1.00 26.86 DIC ATOM 1059 CB GLU 137 15.233 57.832 79.846 1.00 30.23 DIC ATOM 1060 CG GLU 137 15.271 59.120 80.663 1.00 35.53 DIC ATOM 1061 CD GLU 137 16.227 59.028 81.844 1.00 38.87 DIC ATOM 1062 OE1 GLU 137 16.443 57.933 82.435 1.00 40.95 DIC ATOM 1063 OE2 GLU 137 16.785 60.090 82.175 1.00 41.61 DIC ATOM 1064 C GLU 137 16.185 55.598 80.087 1.00 24.31 DIC ATOM 1065 O GLU 137 15.407 54.984 79.365 1.00 25.87 DIC ATOM 1066 N GLY 138 16.766 55.070 81.149 1.00 23.93 DIC ATOM 1067 CA GLY 138 16.451 53.729 81.594 1.00 22.33 DIC ATOM 1068 C GLY 138 16.756 52.535 80.724 1.00 21.12 DIC ATOM 1069 O GLY 138 16.509 51.410 81.164 1.00 22.81 DIC ATOM 1070 N TYR 139 17.289 52.734 79.526 1.00 18.91 DIC ATOM 1071 CA TYR 139 17.555 51.583 78.676 1.00 17.98 DIC ATOM 1072 CB TYR 139 18.002 52.012 77.282 1.00 17.34 DIC ATOM 1073 CG TYR 139 18.291 50.799 76.400 1.00 17.33 DIC ATOM 1074 CD1 TYR 139 17.254 49.968 75.965 1.00 18.26 DIC ATOM 1075 CE1 TYR 139 17.510 48.815 75.222 1.00 16.56 DIC ATOM 1076 CD2 TYR 139 19.602 50.442 76.062 1.00 15.79 DIC ATOM 1077 CE2 TYR 139 19.866 49.284 75.312 1.00 15.54 DIC ATOM 1078 CZ TYR 139 18.813 48.480 74.901 1.00 16.42 DIC ATOM 1079 OH TYR 139 19.045 47.340 74.165 1.00 15.74 DIC ATOM 1080 C TYR 139 18.584 50.596 79.212 1.00 17.11 DIC ATOM 1081 O TYR 139 18.348 49.386 79.242 1.00 17.36 DIC ATOM 1082 N LYS 140 19.744 51.130 79.571 1.00 15.75 DIC ATOM 1083 CA LYS 140 20.865 50.365 80.083 1.00 16.81 DIC ATOM 1084 CB LYS 140 21.894 51.354 80.635 1.00 19.79 DIC ATOM 1085 CG LYS 140 23.223 50.771 80.995 1.00 23.22 DIC ATOM 1086 CD LYS 140 24.253 51.863 81.267 1.00 21.44 DIC ATOM 1087 CE LYS 140 23.904 52.707 82.480 1.00 23.50 DIC ATOM 1088 NZ LYS 140 25.043 53.584 82.849 1.00 22.17 DIC ATOM 1089 C LYS 140 20.404 49.388 81.162 1.00 17.13 DIC ATOM 1090 O LYS 140 20.812 48.226 81.180 1.00 14.56 DIC ATOM 1091 N GLN 141 19.540 49.862 82.053 1.00 16.81 DIC ATOM 1092 CA GLN 141 19.027 49.029 83.130 1.00 18.98 DIC ATOM 1093 CB GLN 141 18.259 49.896 84.137 1.00 19.80 DIC ATOM 1094 CG GLN 141 19.152 50.846 84.948 1.00 18.45 DIC ATOM 1095 CD GLN 141 19.602 52.091 84.178 1.00 20.81 DIC ATOM 1096 OE1 GLN 141 19.304 52.258 82.994 1.00 19.23 DIC ATOM 1097 NE2 GLN 141 20.327 52.972 84.860 1.00 18.11 DIC ATOM 1098 C GLN 141 18.147 47.878 82.624 1.00 19.56 DIC ATOM 1099 O GLN 141 18.071 46.822 83.258 1.00 20.21 DIC ATOM 1100 N LYS 142 17.495 48.070 81.479 1.00 18.99 DIC ATOM 1101 CA LYS 142 16.653 47.019 80.915 1.00 18.42 DIC ATOM 1102 CB LYS 142 15.947 47.503 79.644 1.00 20.49 DIC ATOM 1103 CG LYS 142 14.882 48.562 79.871 1.00 23.32 DIC ATOM 1104 CD LYS 142 14.220 48.950 78.552 1.00 24.72 DIC ATOM 1105 CE LYS 142 13.110 49.968 78.761 1.00 26.12 DIC ATOM 1106 NZ LYS 142 12.037 49.424 79.644 1.00 26.72 DIC ATOM 1107 C LYS 142 17.477 45.778 80.580 1.00 18.39 DIC ATOM 1108 O LYS 142 16.951 44.661 80.557 1.00 17.06 DIC ATOM 1109 N ILE 143 18.764 45.957 80.294 1.00 16.69 DIC ATOM 1110 CA ILE 143 19.569 44.785 79.985 1.00 15.20 DIC ATOM 1111 CB ILE 143 20.389 44.964 78.680 1.00 14.48 DIC ATOM 1112 CG2 ILE 143 19.438 45.218 77.519 1.00 15.42 DIC ATOM 1113 CG1 ILE 143 21.384 46.112 78.811 1.00 14.17 DIC ATOM 1114 CD ILE 143 22.379 46.166 77.652 1.00 14.63 DIC ATOM 1115 C ILE 143 20.471 44.362 81.143 1.00 14.14 DIC ATOM 1116 O ILE 143 21.477 43.685 80.943 1.00 14.10 DIC ATOM 1117 N GLY 144 20.089 44.767 82.355 1.00 14.85 DIC ATOM 1118 CA GLY 144 20.816 44.381 83.557 1.00 13.42 DIC ATOM 1119 C GLY 144 22.048 45.154 83.984 1.00 15.34 DIC ATOM 1120 O GLY 144 22.775 44.721 84.884 1.00 14.31 DIC ATOM 1121 N MSE 145 22.295 46.298 83.361 1.00 14.04 DIC ATOM 1122 CA MSE 145 23.458 47.091 83.720 1.00 15.25 DIC ATOM 1123 CB MSE 145 23.997 47.815 82.485 1.00 14.45 DIC ATOM 1124 CG MSE 145 24.524 46.865 81.415 1.00 15.86 DIC ATOM 1125 SE MSE 145 25.126 47.799 79.831 1.00 16.27 DIC ATOM 1126 CE MSE 145 26.753 48.566 80.498 1.00 14.18 DIC ATOM 1127 C MSE 145 23.115 48.099 84.809 1.00 16.09 DIC ATOM 1128 O MSE 145 21.984 48.585 84.882 1.00 14.76 DIC ATOM 1129 N ALA 146 24.096 48.400 85.655 1.00 17.00 DIC ATOM 1130 CA ALA 146 23.903 49.366 86.728 1.00 18.41 DIC ATOM 1131 CB ALA 146 24.802 49.033 87.906 1.00 18.96 DIC ATOM 1132 C ALA 146 24.238 50.752 86.192 1.00 19.79 DIC ATOM 1133 O ALA 146 24.793 50.885 85.098 1.00 18.39 DIC ATOM 1134 N ASP 147 23.906 51.778 86.971 1.00 19.70 DIC ATOM 1135 CA ASP 147 24.168 53.155 86.576 1.00 20.75 DIC ATOM 1136 CB ASP 147 23.657 54.136 87.632 1.00 24.89 DIC ATOM 1137 CG ASP 147 23.905 55.584 87.242 1.00 28.79 DIC ATOM 1138 OD1 ASP 147 23.171 56.108 86.380 1.00 32.14 DIC ATOM 1139 OD2 ASP 147 24.845 56.199 87.787 1.00 33.35 DIC ATOM 1140 C ASP 147 25.643 53.421 86.355 1.00 18.89 DIC ATOM 1141 O ASP 147 26.007 54.205 85.472 1.00 19.38 DIC ATOM 1142 N GLY 148 26.483 52.771 87.158 1.00 16.62 DIC ATOM 1143 CA GLY 148 27.924 52.959 87.058 1.00 15.83 DIC ATOM 1144 C GLY 148 28.640 52.121 86.013 1.00 14.92 DIC ATOM 1145 O GLY 148 29.852 52.238 85.842 1.00 15.77 DIC ATOM 1146 N GLU 149 27.908 51.257 85.320 1.00 14.62 DIC ATOM 1147 CA GLU 149 28.512 50.434 84.280 1.00 13.91 DIC ATOM 1148 CB GLU 149 27.948 49.015 84.331 1.00 13.40 DIC ATOM 1149 CG GLU 149 28.174 48.342 85.680 1.00 16.25 DIC ATOM 1150 CD GLU 149 27.669 46.912 85.717 1.00 17.21 DIC ATOM 1151 OE1 GLU 149 26.540 46.662 85.246 1.00 17.01 DIC ATOM 1152 OE2 GLU 149 28.403 46.041 86.228 1.00 18.86 DIC ATOM 1153 C GLU 149 28.133 51.128 82.984 1.00 13.92 DIC ATOM 1154 O GLU 149 26.958 51.207 82.635 1.00 14.24 DIC ATOM 1155 N TYR 150 29.131 51.641 82.280 1.00 13.00 DIC ATOM 1156 CA TYR 150 28.880 52.386 81.056 1.00 14.46 DIC ATOM 1157 CB TYR 150 29.968 53.449 80.904 1.00 14.10 DIC ATOM 1158 CG TYR 150 30.069 54.308 82.151 1.00 14.23 DIC ATOM 1159 CD1 TYR 150 31.304 54.579 82.734 1.00 14.50 DIC ATOM 1160 CE1 TYR 150 31.401 55.298 83.924 1.00 15.54 DIC ATOM 1161 CD2 TYR 150 28.920 54.787 82.789 1.00 14.65 DIC ATOM 1162 CE2 TYR 150 29.006 55.510 83.987 1.00 15.14 DIC ATOM 1163 CZ TYR 150 30.256 55.756 84.545 1.00 16.39 DIC ATOM 1164 OH TYR 150 30.373 56.440 85.728 1.00 15.21 DIC ATOM 1165 C TYR 150 28.724 51.555 79.789 1.00 13.06 DIC ATOM 1166 O TYR 150 29.524 50.665 79.495 1.00 12.78 DIC ATOM 1167 N TYR 151 27.663 51.858 79.049 1.00 11.90 DIC ATOM 1168 CA TYR 151 27.351 51.143 77.819 1.00 12.53 DIC ATOM 1169 CB TYR 151 25.931 51.509 77.374 1.00 12.20 DIC ATOM 1170 CG TYR 151 25.352 50.644 76.274 1.00 11.21 DIC ATOM 1171 CD1 TYR 151 25.752 50.802 74.951 1.00 9.91 DIC ATOM 1172 CE1 TYR 151 25.195 50.034 73.930 1.00 10.32 DIC ATOM 1173 CD2 TYR 151 24.373 49.687 76.557 1.00 11.48 DIC ATOM 1174 CE2 TYR 151 23.810 48.911 75.546 1.00 11.82 DIC ATOM 1175 CZ TYR 151 24.225 49.090 74.230 1.00 12.60 DIC ATOM 1176 OH TYR 151 23.668 48.330 73.218 1.00 10.81 DIC ATOM 1177 C TYR 151 28.372 51.512 76.751 1.00 11.38 DIC ATOM 1178 O TYR 151 28.577 52.689 76.458 1.00 11.36 DIC ATOM 1179 N PHE 152 29.041 50.513 76.190 1.00 10.71 DIC ATOM 1180 CA PHE 152 30.030 50.812 75.168 1.00 10.99 DIC ATOM 1181 CB PHE 152 31.337 50.034 75.416 1.00 10.34 DIC ATOM 1182 CG PHE 152 31.193 48.533 75.372 1.00 10.77 DIC ATOM 1183 CD1 PHE 152 30.968 47.802 76.539 1.00 9.58 DIC ATOM 1184 CD2 PHE 152 31.324 47.844 74.166 1.00 10.11 DIC ATOM 1185 CE1 PHE 152 30.879 46.399 76.507 1.00 12.23 DIC ATOM 1186 CE2 PHE 152 31.236 46.445 74.122 1.00 11.41 DIC ATOM 1187 CZ PHE 152 31.015 45.720 75.291 1.00 10.68 DIC ATOM 1188 C PHE 152 29.502 50.541 73.768 1.00 11.13 DIC ATOM 1189 O PHE 152 28.519 49.813 73.597 1.00 12.61 DIC ATOM 1190 N ASN 153 30.131 51.161 72.772 1.00 10.37 DIC ATOM 1191 CA ASN 153 29.732 50.962 71.385 1.00 8.75 DIC ATOM 1192 CB ASN 153 29.969 52.231 70.553 1.00 10.03 DIC ATOM 1193 CG ASN 153 29.579 52.052 69.092 1.00 8.59 DIC ATOM 1194 OD1 ASN 153 30.396 51.662 68.260 1.00 9.43 DIC ATOM 1195 ND2 ASN 153 28.319 52.314 68.785 1.00 10.09 DIC ATOM 1196 C ASN 153 30.560 49.802 70.854 1.00 8.80 DIC ATOM 1197 O ASN 153 31.768 49.738 71.073 1.00 9.14 DIC ATOM 1198 N ALA 154 29.914 48.879 70.154 1.00 9.45 DIC ATOM 1199 CA ALA 154 30.617 47.702 69.651 1.00 10.62 DIC ATOM 1200 CB ALA 154 29.634 46.546 69.518 1.00 11.77 DIC ATOM 1201 C ALA 154 31.368 47.895 68.339 1.00 9.97 DIC ATOM 1202 O ALA 154 31.940 46.944 67.814 1.00 10.61 DIC ATOM 1203 N GLY 155 31.381 49.119 67.818 1.00 8.84 DIC ATOM 1204 CA GLY 155 32.054 49.377 66.553 1.00 9.49 DIC ATOM 1205 C GLY 155 33.575 49.396 66.545 1.00 9.26 DIC ATOM 1206 O GLY 155 34.193 49.248 65.485 1.00 9.60 DIC ATOM 1207 N VAL 156 34.183 49.589 67.715 1.00 8.00 DIC ATOM 1208 CA VAL 156 35.640 49.631 67.849 1.00 6.16 DIC ATOM 1209 CB VAL 156 36.152 51.095 67.977 1.00 8.60 DIC ATOM 1210 CG1 VAL 156 37.667 51.111 68.200 1.00 8.18 DIC ATOM 1211 CG2 VAL 156 35.788 51.887 66.708 1.00 4.42 DIC ATOM 1212 C VAL 156 35.968 48.869 69.120 1.00 7.98 DIC ATOM 1213 O VAL 156 35.711 49.351 70.225 1.00 7.64 DIC ATOM 1214 N LEU 157 36.540 47.679 68.973 1.00 7.93 DIC ATOM 1215 CA LEU 157 36.826 46.861 70.140 1.00 8.32 DIC ATOM 1216 CB LEU 157 35.812 45.714 70.216 1.00 8.82 DIC ATOM 1217 CG LEU 157 34.317 46.025 70.104 1.00 6.30 DIC ATOM 1218 CD1 LEU 157 33.579 44.733 69.815 1.00 3.81 DIC ATOM 1219 CD2 LEU 157 33.804 46.675 71.373 1.00 6.09 DIC ATOM 1220 C LEU 157 38.218 46.259 70.190 1.00 10.43 DIC ATOM 1221 O LEU 157 38.623 45.544 69.270 1.00 10.91 DIC ATOM 1222 N LEU 158 38.948 46.546 71.265 1.00 10.32 DIC ATOM 1223 CA LEU 158 40.270 45.967 71.444 1.00 11.68 DIC ATOM 1224 CB LEU 158 41.172 46.887 72.266 1.00 13.62 DIC ATOM 1225 CG LEU 158 42.617 46.400 72.369 1.00 14.82 DIC ATOM 1226 CD1 LEU 158 43.239 46.368 70.981 1.00 14.39 DIC ATOM 1227 CD2 LEU 158 43.409 47.323 73.283 1.00 16.11 DIC ATOM 1228 C LEU 158 39.929 44.705 72.227 1.00 12.27 DIC ATOM 1229 O LEU 158 39.531 44.767 73.396 1.00 13.47 DIC ATOM 1230 N ILE 159 40.082 43.557 71.586 1.00 12.60 DIC ATOM 1231 CA ILE 159 39.707 42.300 72.216 1.00 12.69 DIC ATOM 1232 CB ILE 159 38.874 41.471 71.212 1.00 12.19 DIC ATOM 1233 CG2 ILE 159 38.528 40.093 71.792 1.00 9.38 DIC ATOM 1234 CG1 ILE 159 37.630 42.286 70.843 1.00 9.30 DIC ATOM 1235 CD ILE 159 36.700 41.635 69.869 1.00 13.02 DIC ATOM 1236 C ILE 159 40.811 41.440 72.816 1.00 13.96 DIC ATOM 1237 O ILE 159 41.850 41.185 72.200 1.00 12.79 DIC ATOM 1238 N ASN 160 40.570 41.009 74.048 1.00 14.07 DIC ATOM 1239 CA ASN 160 41.498 40.142 74.757 1.00 13.56 DIC ATOM 1240 CB ASN 160 41.284 40.294 76.260 1.00 14.31 DIC ATOM 1241 CG ASN 160 42.227 39.443 77.074 1.00 13.83 DIC ATOM 1242 OD1 ASN 160 42.806 38.490 76.571 1.00 13.36 DIC ATOM 1243 ND2 ASN 160 42.374 39.778 78.347 1.00 12.66 DIC ATOM 1244 C ASN 160 41.120 38.730 74.301 1.00 13.20 DIC ATOM 1245 O ASN 160 40.485 37.980 75.041 1.00 12.35 DIC ATOM 1246 N LEU 161 41.497 38.380 73.073 1.00 14.48 DIC ATOM 1247 CA LEU 161 41.173 37.071 72.506 1.00 14.41 DIC ATOM 1248 CB LEU 161 41.772 36.927 71.103 1.00 15.27 DIC ATOM 1249 CG LEU 161 40.849 37.142 69.902 1.00 19.60 DIC ATOM 1250 CD1 LEU 161 41.625 36.854 68.629 1.00 17.54 DIC ATOM 1251 CD2 LEU 161 39.625 36.239 69.998 1.00 18.80 DIC ATOM 1252 C LEU 161 41.601 35.873 73.345 1.00 14.82 DIC ATOM 1253 O LEU 161 40.904 34.857 73.383 1.00 12.20 DIC ATOM 1254 N LYS 162 42.762 35.973 73.982 1.00 16.27 DIC ATOM 1255 CA LYS 162 43.248 34.885 74.819 1.00 18.17 DIC ATOM 1256 CB LYS 162 44.579 35.269 75.472 1.00 23.17 DIC ATOM 1257 CG LYS 162 45.039 34.285 76.535 1.00 28.53 DIC ATOM 1258 CD LYS 162 46.494 34.495 76.924 1.00 32.40 DIC ATOM 1259 CE LYS 162 47.429 33.990 75.829 1.00 36.43 DIC ATOM 1260 NZ LYS 162 48.845 33.936 76.294 1.00 38.35 DIC ATOM 1261 C LYS 162 42.204 34.572 75.891 1.00 18.73 DIC ATOM 1262 O LYS 162 41.927 33.406 76.178 1.00 17.49 DIC ATOM 1263 N LYS 163 41.622 35.618 76.481 1.00 16.83 DIC ATOM 1264 CA LYS 163 40.603 35.431 77.508 1.00 15.63 DIC ATOM 1265 CB LYS 163 40.269 36.762 78.188 1.00 14.80 DIC ATOM 1266 CG LYS 163 39.303 36.629 79.363 1.00 16.56 DIC ATOM 1267 CD LYS 163 39.014 37.984 79.999 1.00 17.80 DIC ATOM 1268 CE LYS 163 38.043 37.863 81.172 1.00 19.19 DIC ATOM 1269 NZ LYS 163 38.560 36.924 82.210 1.00 24.46 DIC ATOM 1270 C LYS 163 39.334 34.830 76.891 1.00 15.48 DIC ATOM 1271 O LYS 163 38.760 33.888 77.436 1.00 15.56 DIC ATOM 1272 N TRP 164 38.896 35.376 75.758 1.00 13.99 DIC ATOM 1273 CA TRP 164 37.703 34.857 75.088 1.00 14.31 DIC ATOM 1274 CB TRP 164 37.453 35.598 73.773 1.00 12.76 DIC ATOM 1275 CG TRP 164 36.885 36.979 73.909 1.00 12.61 DIC ATOM 1276 CD2 TRP 164 35.948 37.604 73.024 1.00 11.45 DIC ATOM 1277 CE2 TRP 164 35.742 38.923 73.493 1.00 10.90 DIC ATOM 1278 CE3 TRP 164 35.265 37.179 71.876 1.00 11.56 DIC ATOM 1279 CD1 TRP 164 37.200 37.914 74.855 1.00 12.23 DIC ATOM 1280 NE1 TRP 164 36.518 39.084 74.612 1.00 12.19 DIC ATOM 1281 CZ2 TRP 164 34.880 39.823 72.852 1.00 10.67 DIC ATOM 1282 CZ3 TRP 164 34.406 38.076 71.238 1.00 10.59 DIC ATOM 1283 CH2 TRP 164 34.224 39.382 71.729 1.00 11.25 DIC ATOM 1284 C TRP 164 37.828 33.359 74.782 1.00 14.32 DIC ATOM 1285 O TRP 164 36.862 32.607 74.925 1.00 12.37 DIC ATOM 1286 N ARG 165 39.009 32.927 74.349 1.00 14.03 DIC ATOM 1287 CA ARG 165 39.191 31.519 74.008 1.00 15.65 DIC ATOM 1288 CB ARG 165 40.515 31.307 73.260 1.00 17.22 DIC ATOM 1289 CG ARG 165 40.498 31.881 71.833 1.00 18.70 DIC ATOM 1290 CD ARG 165 41.599 31.285 70.945 1.00 20.78 DIC ATOM 1291 NE ARG 165 42.933 31.672 71.394 1.00 20.86 DIC ATOM 1292 CZ ARG 165 43.595 32.737 70.954 1.00 22.03 DIC ATOM 1293 NH1 ARG 165 44.802 33.012 71.433 1.00 22.53 DIC ATOM 1294 NH2 ARG 165 43.064 33.513 70.018 1.00 23.03 DIC ATOM 1295 C ARG 165 39.084 30.589 75.213 1.00 16.07 DIC ATOM 1296 O ARG 165 38.959 29.377 75.061 1.00 15.48 DIC ATOM 1297 N ARG 166 39.105 31.159 76.411 1.00 17.98 DIC ATOM 1298 CA ARG 166 38.971 30.364 77.623 1.00 18.39 DIC ATOM 1299 CB ARG 166 39.585 31.090 78.822 1.00 21.23 DIC ATOM 1300 CG ARG 166 41.090 31.236 78.787 1.00 23.66 DIC ATOM 1301 CD ARG 166 41.585 31.922 80.051 1.00 24.40 DIC ATOM 1302 NE ARG 166 43.031 32.101 80.017 1.00 28.45 DIC ATOM 1303 CZ ARG 166 43.644 33.276 79.929 1.00 28.36 DIC ATOM 1304 NH1 ARG 166 42.940 34.403 79.870 1.00 28.09 DIC ATOM 1305 NH2 ARG 166 44.968 33.321 79.885 1.00 30.30 DIC ATOM 1306 C ARG 166 37.489 30.141 77.906 1.00 18.07 DIC ATOM 1307 O ARG 166 37.133 29.484 78.879 1.00 16.59 DIC ATOM 1308 N HIS 167 36.625 30.688 77.056 1.00 16.94 DIC ATOM 1309 CA HIS 167 35.188 30.563 77.273 1.00 16.99 DIC ATOM 1310 CB HIS 167 34.652 31.848 77.920 1.00 17.50 DIC ATOM 1311 CG HIS 167 35.333 32.218 79.201 1.00 17.81 DIC ATOM 1312 CD2 HIS 167 36.422 32.989 79.441 1.00 16.88 DIC ATOM 1313 ND1 HIS 167 34.896 31.780 80.434 1.00 19.03 DIC ATOM 1314 CE1 HIS 167 35.683 32.266 81.378 1.00 19.16 DIC ATOM 1315 NE2 HIS 167 36.617 33.004 80.802 1.00 18.25 DIC ATOM 1316 C HIS 167 34.413 30.311 75.987 1.00 17.81 DIC ATOM 1317 O HIS 167 34.939 30.471 74.884 1.00 18.91 DIC ATOM 1318 N ASP 168 33.154 29.916 76.141 1.00 16.56 DIC ATOM 1319 CA ASP 168 32.287 29.682 74.997 1.00 15.52 DIC ATOM 1320 CB ASP 168 31.461 28.406 75.187 1.00 14.57 DIC ATOM 1321 CG ASP 168 30.727 28.001 73.921 1.00 16.35 DIC ATOM 1322 OD1 ASP 168 30.399 26.806 73.768 1.00 16.74 DIC ATOM 1323 OD2 ASP 168 30.473 28.886 73.075 1.00 16.42 DIC ATOM 1324 C ASP 168 31.377 30.900 74.878 1.00 14.56 DIC ATOM 1325 O ASP 168 30.244 30.905 75.361 1.00 15.15 DIC ATOM 1326 N ILE 169 31.893 31.934 74.221 1.00 14.02 DIC ATOM 1327 CA ILE 169 31.169 33.186 74.040 1.00 14.18 DIC ATOM 1328 CB ILE 169 32.044 34.220 73.308 1.00 13.81 DIC ATOM 1329 CG2 ILE 169 31.311 35.554 73.224 1.00 12.37 DIC ATOM 1330 CG1 ILE 169 33.388 34.373 74.032 1.00 14.52 DIC ATOM 1331 CD ILE 169 33.270 34.779 75.498 1.00 15.00 DIC ATOM 1332 C ILE 169 29.849 33.038 73.281 1.00 13.80 DIC ATOM 1333 O ILE 169 28.873 33.729 73.584 1.00 12.98 DIC ATOM 1334 N PHE 170 29.809 32.145 72.300 1.00 14.34 DIC ATOM 1335 CA PHE 170 28.576 31.957 71.539 1.00 14.12 DIC ATOM 1336 CB PHE 170 28.818 31.075 70.317 1.00 15.04 DIC ATOM 1337 CG PHE 170 27.591 30.866 69.482 1.00 16.16 DIC ATOM 1338 CD1 PHE 170 26.936 29.636 69.476 1.00 18.23 DIC ATOM 1339 CD2 PHE 170 27.067 31.909 68.732 1.00 17.64 DIC ATOM 1340 CE1 PHE 170 25.770 29.449 68.733 1.00 19.07 DIC ATOM 1341 CE2 PHE 170 25.903 31.738 67.987 1.00 18.59 DIC ATOM 1342 CZ PHE 170 25.250 30.502 67.987 1.00 19.29 DIC ATOM 1343 C PHE 170 27.485 31.343 72.412 1.00 14.67 DIC ATOM 1344 O PHE 170 26.321 31.738 72.342 1.00 14.40 DIC ATOM 1345 N LYS 171 27.860 30.380 73.244 1.00 14.30 DIC ATOM 1346 CA LYS 171 26.887 29.755 74.120 1.00 15.30 DIC ATOM 1347 CB LYS 171 27.521 28.566 74.841 1.00 17.59 DIC ATOM 1348 CG LYS 171 26.511 27.636 75.474 1.00 22.27 DIC ATOM 1349 CD LYS 171 27.160 26.339 75.928 1.00 24.47 DIC ATOM 1350 CE LYS 171 27.627 25.502 74.744 1.00 27.47 DIC ATOM 1351 NZ LYS 171 28.299 24.238 75.192 1.00 31.51 DIC ATOM 1352 C LYS 171 26.396 30.802 75.121 1.00 14.40 DIC ATOM 1353 O LYS 171 25.197 30.933 75.355 1.00 15.04 DIC ATOM 1354 N MSE 172 27.327 31.553 75.702 1.00 12.53 DIC ATOM 1355 CA MSE 172 26.969 32.599 76.656 1.00 12.42 DIC ATOM 1356 CB MSE 172 28.232 33.280 77.203 1.00 12.59 DIC ATOM 1357 CG MSE 172 29.087 32.407 78.120 1.00 14.48 DIC ATOM 1358 SE MSE 172 30.875 33.131 78.357 1.00 19.27 DIC ATOM 1359 CE MSE 172 30.437 34.845 79.143 1.00 17.17 DIC ATOM 1360 C MSE 172 26.082 33.640 75.963 1.00 12.96 DIC ATOM 1361 O MSE 172 25.175 34.199 76.583 1.00 12.64 DIC ATOM 1362 N SER 173 26.347 33.892 74.679 1.00 11.38 DIC ATOM 1363 CA SER 173 25.566 34.863 73.914 1.00 11.90 DIC ATOM 1364 CB SER 173 26.205 35.118 72.542 1.00 12.42 DIC ATOM 1365 OG SER 173 27.411 35.867 72.657 1.00 11.32 DIC ATOM 1366 C SER 173 24.141 34.356 73.724 1.00 12.64 DIC ATOM 1367 O SER 173 23.172 35.079 73.988 1.00 9.99 DIC ATOM 1368 N SER 174 24.026 33.107 73.275 1.00 12.51 DIC ATOM 1369 CA SER 174 22.730 32.489 73.040 1.00 13.32 DIC ATOM 1370 CB SER 174 22.921 31.065 72.510 1.00 13.27 DIC ATOM 1371 OG SER 174 23.581 31.100 71.259 1.00 14.11 DIC ATOM 1372 C SER 174 21.861 32.472 74.292 1.00 13.57 DIC ATOM 1373 O SER 174 20.647 32.711 74.221 1.00 13.23 DIC ATOM 1374 N GLU 175 22.480 32.187 75.434 1.00 13.02 DIC ATOM 1375 CA GLU 175 21.758 32.151 76.698 1.00 14.86 DIC ATOM 1376 CB GLU 175 22.638 31.542 77.797 1.00 17.57 DIC ATOM 1377 CG GLU 175 23.168 30.152 77.451 1.00 22.53 DIC ATOM 1378 CD GLU 175 23.838 29.457 78.626 1.00 25.32 DIC ATOM 1379 OE1 GLU 175 24.535 30.136 79.413 1.00 26.06 DIC ATOM 1380 OE2 GLU 175 23.673 28.222 78.753 1.00 28.49 DIC ATOM 1381 C GLU 175 21.311 33.557 77.109 1.00 14.41 DIC ATOM 1382 O GLU 175 20.216 33.737 77.648 1.00 15.15 DIC ATOM 1383 N TRP 176 22.158 34.550 76.851 1.00 14.00 DIC ATOM 1384 CA TRP 176 21.832 35.932 77.198 1.00 13.86 DIC ATOM 1385 CB TRP 176 23.041 36.841 76.957 1.00 14.76 DIC ATOM 1386 CG TRP 176 22.907 38.186 77.599 1.00 14.73 DIC ATOM 1387 CD2 TRP 176 22.383 39.375 76.999 1.00 15.10 DIC ATOM 1388 CE2 TRP 176 22.400 40.383 77.987 1.00 15.08 DIC ATOM 1389 CE3 TRP 176 21.896 39.685 75.725 1.00 14.14 DIC ATOM 1390 CD1 TRP 176 23.213 38.511 78.884 1.00 15.31 DIC ATOM 1391 NE1 TRP 176 22.912 39.829 79.128 1.00 14.86 DIC ATOM 1392 CZ2 TRP 176 21.949 41.684 77.738 1.00 15.02 DIC ATOM 1393 CZ3 TRP 176 21.446 40.979 75.479 1.00 13.42 DIC ATOM 1394 CH2 TRP 176 21.476 41.960 76.480 1.00 14.16 DIC ATOM 1395 C TRP 176 20.653 36.396 76.342 1.00 14.32 DIC ATOM 1396 O TRP 176 19.709 37.024 76.842 1.00 14.65 DIC ATOM 1397 N VAL 177 20.707 36.082 75.050 1.00 13.88 DIC ATOM 1398 CA VAL 177 19.633 36.463 74.144 1.00 13.78 DIC ATOM 1399 CB VAL 177 19.917 36.021 72.692 1.00 13.94 DIC ATOM 1400 CG1 VAL 177 18.673 36.235 71.837 1.00 14.54 DIC ATOM 1401 CG2 VAL 177 21.072 36.828 72.112 1.00 11.49 DIC ATOM 1402 C VAL 177 18.320 35.839 74.601 1.00 15.27 DIC ATOM 1403 O VAL 177 17.269 36.476 74.560 1.00 13.41 DIC ATOM 1404 N GLU 178 18.373 34.591 75.043 1.00 17.23 DIC ATOM 1405 CA GLU 178 17.157 33.933 75.491 1.00 20.02 DIC ATOM 1406 CB GLU 178 17.469 32.505 75.952 1.00 22.23 DIC ATOM 1407 CG GLU 178 16.236 31.648 76.208 1.00 27.72 DIC ATOM 1408 CD GLU 178 15.214 31.727 75.078 1.00 29.81 DIC ATOM 1409 OE1 GLU 178 15.590 31.535 73.898 1.00 31.17 DIC ATOM 1410 OE2 GLU 178 14.027 31.979 75.376 1.00 32.50 DIC ATOM 1411 C GLU 178 16.549 34.735 76.636 1.00 20.30 DIC ATOM 1412 O GLU 178 15.328 34.848 76.758 1.00 20.62 DIC ATOM 1413 N GLN 179 17.416 35.320 77.453 1.00 19.19 DIC ATOM 1414 CA GLN 179 16.988 36.093 78.609 1.00 21.07 DIC ATOM 1415 CB GLN 179 18.136 36.120 79.625 1.00 23.36 DIC ATOM 1416 CG GLN 179 17.829 36.793 80.943 1.00 29.17 DIC ATOM 1417 CD GLN 179 19.050 36.865 81.852 1.00 33.38 DIC ATOM 1418 OE1 GLN 179 18.995 37.432 82.947 1.00 35.19 DIC ATOM 1419 NE2 GLN 179 20.163 36.290 81.396 1.00 34.26 DIC ATOM 1420 C GLN 179 16.516 37.524 78.313 1.00 19.81 DIC ATOM 1421 O GLN 179 15.593 38.018 78.956 1.00 18.51 DIC ATOM 1422 N TYR 180 17.125 38.183 77.333 1.00 18.69 DIC ATOM 1423 CA TYR 180 16.758 39.561 77.038 1.00 17.26 DIC ATOM 1424 CB TYR 180 17.962 40.469 77.277 1.00 17.36 DIC ATOM 1425 CG TYR 180 18.421 40.529 78.710 1.00 18.17 DIC ATOM 1426 CD1 TYR 180 19.325 39.598 79.214 1.00 18.19 DIC ATOM 1427 CE1 TYR 180 19.773 39.675 80.528 1.00 19.56 DIC ATOM 1428 CD2 TYR 180 17.966 41.535 79.560 1.00 19.48 DIC ATOM 1429 CE2 TYR 180 18.404 41.618 80.873 1.00 19.98 DIC ATOM 1430 CZ TYR 180 19.310 40.685 81.351 1.00 19.10 DIC ATOM 1431 OH TYR 180 19.760 40.772 82.650 1.00 21.76 DIC ATOM 1432 C TYR 180 16.206 39.861 75.651 1.00 17.56 DIC ATOM 1433 O TYR 180 16.068 41.030 75.288 1.00 16.75 DIC ATOM 1434 N LYS 181 15.886 38.826 74.884 1.00 17.25 DIC ATOM 1435 CA LYS 181 15.382 39.004 73.523 1.00 19.55 DIC ATOM 1436 CB LYS 181 15.086 37.636 72.898 1.00 22.09 DIC ATOM 1437 CG LYS 181 13.950 36.875 73.566 1.00 24.42 DIC ATOM 1438 CD LYS 181 13.778 35.491 72.946 1.00 28.02 DIC ATOM 1439 CE LYS 181 12.475 34.847 73.395 1.00 28.32 DIC ATOM 1440 NZ LYS 181 12.358 34.833 74.878 1.00 31.53 DIC ATOM 1441 C LYS 181 14.150 39.902 73.367 1.00 20.33 DIC ATOM 1442 O LYS 181 13.940 40.489 72.304 1.00 19.96 DIC ATOM 1443 N ASP 182 13.336 40.012 74.410 1.00 19.39 DIC ATOM 1444 CA ASP 182 12.132 40.830 74.320 1.00 21.97 DIC ATOM 1445 CB ASP 182 11.053 40.288 75.258 1.00 23.67 DIC ATOM 1446 CG ASP 182 10.476 38.965 74.785 1.00 26.84 DIC ATOM 1447 OD1 ASP 182 9.781 38.308 75.587 1.00 29.25 DIC ATOM 1448 OD2 ASP 182 10.703 38.585 73.614 1.00 27.07 DIC ATOM 1449 C ASP 182 12.368 42.298 74.634 1.00 21.11 DIC ATOM 1450 O ASP 182 11.472 43.121 74.460 1.00 21.52 DIC ATOM 1451 N VAL 183 13.568 42.632 75.096 1.00 19.54 DIC ATOM 1452 CA VAL 183 13.861 44.015 75.435 1.00 18.64 DIC ATOM 1453 CB VAL 183 14.093 44.160 76.968 1.00 20.70 DIC ATOM 1454 CG1 VAL 183 15.332 43.388 77.396 1.00 19.44 DIC ATOM 1455 CG2 VAL 183 14.214 45.617 77.341 1.00 24.74 DIC ATOM 1456 C VAL 183 15.050 44.606 74.682 1.00 18.43 DIC ATOM 1457 O VAL 183 15.104 45.820 74.462 1.00 18.40 DIC ATOM 1458 N MSE 184 15.998 43.766 74.276 1.00 16.59 DIC ATOM 1459 CA MSE 184 17.173 44.276 73.573 1.00 15.96 DIC ATOM 1460 CB MSE 184 18.173 43.135 73.278 1.00 17.24 DIC ATOM 1461 CG MSE 184 17.620 41.917 72.564 1.00 18.77 DIC ATOM 1462 SE MSE 184 18.898 40.440 72.634 1.00 17.57 DIC ATOM 1463 CE MSE 184 20.063 40.984 71.194 1.00 13.79 DIC ATOM 1464 C MSE 184 16.804 45.050 72.305 1.00 15.73 DIC ATOM 1465 O MSE 184 15.940 44.637 71.525 1.00 13.50 DIC ATOM 1466 N GLN 185 17.460 46.195 72.125 1.00 13.82 DIC ATOM 1467 CA GLN 185 17.207 47.074 70.989 1.00 13.45 DIC ATOM 1468 CB GLN 185 16.781 48.460 71.496 1.00 15.92 DIC ATOM 1469 CG GLN 185 15.485 48.468 72.306 1.00 15.22 DIC ATOM 1470 CD GLN 185 15.126 49.847 72.864 1.00 18.20 DIC ATOM 1471 OE1 GLN 185 15.648 50.875 72.417 1.00 16.73 DIC ATOM 1472 NE2 GLN 185 14.215 49.870 73.836 1.00 15.67 DIC ATOM 1473 C GLN 185 18.426 47.231 70.084 1.00 13.75 DIC ATOM 1474 O GLN 185 18.301 47.694 68.945 1.00 12.35 DIC ATOM 1475 N TYR 186 19.602 46.849 70.580 1.00 10.80 DIC ATOM 1476 CA TYR 186 20.809 47.014 69.785 1.00 12.98 DIC ATOM 1477 CB TYR 186 21.742 48.010 70.479 1.00 14.55 DIC ATOM 1478 CG TYR 186 21.067 49.351 70.690 1.00 15.13 DIC ATOM 1479 CD1 TYR 186 20.569 49.720 71.941 1.00 13.69 DIC ATOM 1480 CE1 TYR 186 19.868 50.918 72.116 1.00 14.58 DIC ATOM 1481 CD2 TYR 186 20.854 50.218 69.616 1.00 17.25 DIC ATOM 1482 CE2 TYR 186 20.152 51.414 69.778 1.00 17.83 DIC ATOM 1483 CZ TYR 186 19.662 51.756 71.030 1.00 16.39 DIC ATOM 1484 OH TYR 186 18.958 52.928 71.182 1.00 17.08 DIC ATOM 1485 C TYR 186 21.564 45.764 69.345 1.00 11.95 DIC ATOM 1486 O TYR 186 22.758 45.813 69.056 1.00 10.67 DIC ATOM 1487 N GLN 187 20.853 44.644 69.313 1.00 10.94 DIC ATOM 1488 CA GLN 187 21.400 43.393 68.813 1.00 10.45 DIC ATOM 1489 CB GLN 187 21.435 43.521 67.281 1.00 11.05 DIC ATOM 1490 CG GLN 187 20.042 43.956 66.773 1.00 12.55 DIC ATOM 1491 CD GLN 187 19.927 44.215 65.279 1.00 13.86 DIC ATOM 1492 OE1 GLN 187 18.821 44.351 64.766 1.00 16.40 DIC ATOM 1493 NE2 GLN 187 21.048 44.293 64.582 1.00 12.57 DIC ATOM 1494 C GLN 187 22.735 42.929 69.407 1.00 9.77 DIC ATOM 1495 O GLN 187 22.850 42.793 70.627 1.00 9.45 DIC ATOM 1496 N ASP 188 23.741 42.683 68.568 1.00 8.20 DIC ATOM 1497 CA ASP 188 25.030 42.205 69.071 1.00 8.35 DIC ATOM 1498 CB ASP 188 25.999 41.978 67.916 1.00 9.13 DIC ATOM 1499 CG ASP 188 26.220 43.224 67.111 1.00 12.26 DIC ATOM 1500 OD1 ASP 188 25.312 43.586 66.337 1.00 13.14 DIC ATOM 1501 OD2 ASP 188 27.286 43.846 67.269 1.00 10.65 DIC ATOM 1502 C ASP 188 25.674 43.146 70.089 1.00 9.52 DIC ATOM 1503 O ASP 188 26.453 42.720 70.950 1.00 8.45 DIC ATOM 1504 N GLN 189 25.354 44.428 69.992 1.00 9.27 DIC ATOM 1505 CA GLN 189 25.910 45.409 70.915 1.00 9.53 DIC ATOM 1506 CB GLN 189 25.548 46.816 70.433 1.00 11.21 DIC ATOM 1507 CG GLN 189 26.252 47.950 71.140 1.00 13.73 DIC ATOM 1508 CD GLN 189 26.138 49.248 70.346 1.00 15.81 DIC ATOM 1509 OE1 GLN 189 27.060 49.627 69.622 1.00 13.26 DIC ATOM 1510 NE2 GLN 189 24.989 49.919 70.461 1.00 13.80 DIC ATOM 1511 C GLN 189 25.386 45.156 72.333 1.00 9.28 DIC ATOM 1512 O GLN 189 26.136 45.251 73.300 1.00 7.78 DIC ATOM 1513 N ASP 190 24.100 44.828 72.457 1.00 9.50 DIC ATOM 1514 CA ASP 190 23.521 44.542 73.771 1.00 10.89 DIC ATOM 1515 CB ASP 190 22.021 44.259 73.665 1.00 9.92 DIC ATOM 1516 CG ASP 190 21.208 45.499 73.357 1.00 11.74 DIC ATOM 1517 OD1 ASP 190 20.197 45.360 72.639 1.00 10.56 DIC ATOM 1518 OD2 ASP 190 21.570 46.600 73.841 1.00 9.10 DIC ATOM 1519 C ASP 190 24.186 43.310 74.362 1.00 9.43 DIC ATOM 1520 O ASP 190 24.483 43.263 75.553 1.00 10.61 DIC ATOM 1521 N ILE 191 24.389 42.302 73.524 1.00 8.72 DIC ATOM 1522 CA ILE 191 24.998 41.061 73.970 1.00 8.21 DIC ATOM 1523 CB ILE 191 25.125 40.056 72.811 1.00 8.37 DIC ATOM 1524 CG2 ILE 191 25.797 38.766 73.316 1.00 6.32 DIC ATOM 1525 CG1 ILE 191 23.737 39.736 72.252 1.00 6.91 DIC ATOM 1526 CD ILE 191 23.765 38.864 71.004 1.00 6.73 DIC ATOM 1527 C ILE 191 26.368 41.277 74.590 1.00 9.22 DIC ATOM 1528 O ILE 191 26.640 40.794 75.695 1.00 9.62 DIC ATOM 1529 N LEU 192 27.229 42.011 73.889 1.00 9.09 DIC ATOM 1530 CA LEU 192 28.574 42.276 74.391 1.00 9.40 DIC ATOM 1531 CB LEU 192 29.376 43.060 73.343 1.00 9.83 DIC ATOM 1532 CG LEU 192 29.588 42.326 72.011 1.00 11.31 DIC ATOM 1533 CD1 LEU 192 29.942 43.307 70.901 1.00 12.97 DIC ATOM 1534 CD2 LEU 192 30.678 41.286 72.188 1.00 12.52 DIC ATOM 1535 C LEU 192 28.529 43.047 75.715 1.00 11.04 DIC ATOM 1536 O LEU 192 29.272 42.734 76.652 1.00 9.18 DIC ATOM 1537 N ASN 193 27.662 44.053 75.797 1.00 10.74 DIC ATOM 1538 CA ASN 193 27.547 44.847 77.024 1.00 12.24 DIC ATOM 1539 CB ASN 193 26.619 46.054 76.808 1.00 10.61 DIC ATOM 1540 CG ASN 193 27.362 47.284 76.280 1.00 13.95 DIC ATOM 1541 OD1 ASN 193 28.031 47.991 77.039 1.00 12.61 DIC ATOM 1542 ND2 ASN 193 27.251 47.536 74.974 1.00 10.56 DIC ATOM 1543 C ASN 193 27.010 43.986 78.162 1.00 12.42 DIC ATOM 1544 O ASN 193 27.515 44.039 79.284 1.00 14.38 DIC ATOM 1545 N GLY 194 25.981 43.198 77.872 1.00 12.71 DIC ATOM 1546 CA GLY 194 25.407 42.348 78.898 1.00 13.05 DIC ATOM 1547 C GLY 194 26.403 41.342 79.443 1.00 13.73 DIC ATOM 1548 O GLY 194 26.541 41.172 80.656 1.00 12.77 DIC ATOM 1549 N LEU 195 27.122 40.679 78.547 1.00 12.99 DIC ATOM 1550 CA LEU 195 28.086 39.674 78.969 1.00 13.81 DIC ATOM 1551 CB LEU 195 28.533 38.826 77.769 1.00 11.07 DIC ATOM 1552 CG LEU 195 27.562 37.911 77.016 1.00 11.26 DIC ATOM 1553 CD1 LEU 195 28.303 37.265 75.841 1.00 8.90 DIC ATOM 1554 CD2 LEU 195 27.024 36.820 77.938 1.00 11.82 DIC ATOM 1555 C LEU 195 29.339 40.199 79.675 1.00 13.59 DIC ATOM 1556 O LEU 195 29.822 39.580 80.620 1.00 12.85 DIC ATOM 1557 N PHE 196 29.860 41.341 79.235 1.00 12.78 DIC ATOM 1558 CA PHE 196 31.110 41.842 79.797 1.00 12.08 DIC ATOM 1559 CB PHE 196 32.064 42.204 78.652 1.00 13.05 DIC ATOM 1560 CG PHE 196 32.214 41.119 77.624 1.00 13.16 DIC ATOM 1561 CD1 PHE 196 32.244 39.780 78.004 1.00 10.72 DIC ATOM 1562 CD2 PHE 196 32.359 41.436 76.275 1.00 13.59 DIC ATOM 1563 CE1 PHE 196 32.419 38.766 77.058 1.00 13.82 DIC ATOM 1564 CE2 PHE 196 32.534 40.430 75.318 1.00 12.70 DIC ATOM 1565 CZ PHE 196 32.565 39.095 75.709 1.00 11.81 DIC ATOM 1566 C PHE 196 31.071 42.993 80.786 1.00 13.04 DIC ATOM 1567 O PHE 196 32.125 43.434 81.257 1.00 11.71 DIC ATOM 1568 N LYS 197 29.875 43.480 81.095 1.00 11.55 DIC ATOM 1569 CA LYS 197 29.731 44.577 82.032 1.00 13.00 DIC ATOM 1570 CB LYS 197 28.250 44.784 82.381 1.00 12.60 DIC ATOM 1571 CG LYS 197 27.540 43.582 83.016 1.00 13.14 DIC ATOM 1572 CD LYS 197 26.063 43.899 83.223 1.00 11.03 DIC ATOM 1573 CE LYS 197 25.316 42.798 83.972 1.00 14.35 DIC ATOM 1574 NZ LYS 197 25.265 41.519 83.214 1.00 14.09 DIC ATOM 1575 C LYS 197 30.545 44.286 83.287 1.00 14.20 DIC ATOM 1576 O LYS 197 30.494 43.182 83.826 1.00 14.43 DIC ATOM 1577 N GLY 198 31.319 45.272 83.731 1.00 15.83 DIC ATOM 1578 CA GLY 198 32.146 45.094 84.914 1.00 16.30 DIC ATOM 1579 C GLY 198 33.546 44.622 84.566 1.00 16.73 DIC ATOM 1580 O GLY 198 34.457 44.678 85.395 1.00 15.89 DIC ATOM 1581 N GLY 199 33.718 44.158 83.330 1.00 15.83 DIC ATOM 1582 CA GLY 199 35.014 43.676 82.886 1.00 15.74 DIC ATOM 1583 C GLY 199 35.395 44.315 81.563 1.00 17.97 DIC ATOM 1584 O GLY 199 35.854 43.644 80.641 1.00 16.51 DIC ATOM 1585 N VAL 200 35.191 45.625 81.484 1.00 16.42 DIC ATOM 1586 CA VAL 200 35.498 46.397 80.292 1.00 17.21 DIC ATOM 1587 CB VAL 200 34.219 47.034 79.696 1.00 16.55 DIC ATOM 1588 CG1 VAL 200 34.586 47.977 78.547 1.00 19.60 DIC ATOM 1589 CG2 VAL 200 33.275 45.951 79.204 1.00 17.01 DIC ATOM 1590 C VAL 200 36.471 47.533 80.596 1.00 16.86 DIC ATOM 1591 O VAL 200 36.337 48.228 81.601 1.00 16.58 DIC ATOM 1592 N CYS 201 37.454 47.708 79.720 1.00 16.59 DIC ATOM 1593 CA CYS 201 38.412 48.793 79.853 1.00 17.05 DIC ATOM 1594 CB CYS 201 39.802 48.345 79.391 1.00 19.85 DIC ATOM 1595 SG CYS 201 41.031 49.677 79.319 1.00 29.46 DIC ATOM 1596 C CYS 201 37.847 49.848 78.912 1.00 15.68 DIC ATOM 1597 O CYS 201 37.519 49.543 77.765 1.00 15.05 DIC ATOM 1598 N TYR 202 37.697 51.079 79.386 1.00 15.85 DIC ATOM 1599 CA TYR 202 37.132 52.114 78.529 1.00 14.50 DIC ATOM 1600 CB TYR 202 36.236 53.054 79.333 1.00 15.59 DIC ATOM 1601 CG TYR 202 35.102 52.377 80.061 1.00 17.50 DIC ATOM 1602 CD1 TYR 202 35.173 52.162 81.434 1.00 17.93 DIC ATOM 1603 CE1 TYR 202 34.125 51.583 82.124 1.00 19.81 DIC ATOM 1604 CD2 TYR 202 33.944 51.984 79.388 1.00 18.20 DIC ATOM 1605 CE2 TYR 202 32.882 51.396 80.072 1.00 19.70 DIC ATOM 1606 CZ TYR 202 32.983 51.205 81.447 1.00 21.08 DIC ATOM 1607 OH TYR 202 31.941 50.670 82.163 1.00 20.73 DIC ATOM 1608 C TYR 202 38.206 52.933 77.831 1.00 14.93 DIC ATOM 1609 O TYR 202 39.161 53.372 78.462 1.00 15.02 DIC ATOM 1610 N ALA 203 38.038 53.130 76.525 1.00 13.78 DIC ATOM 1611 CA ALA 203 38.980 53.913 75.725 1.00 12.83 DIC ATOM 1612 CB ALA 203 39.210 53.243 74.377 1.00 11.34 DIC ATOM 1613 C ALA 203 38.402 55.306 75.514 1.00 13.01 DIC ATOM 1614 O ALA 203 37.196 55.506 75.643 1.00 12.43 DIC ATOM 1615 N ASN 204 39.257 56.272 75.195 1.00 12.21 DIC ATOM 1616 CA ASN 204 38.774 57.628 74.962 1.00 11.59 DIC ATOM 1617 CB ASN 204 39.936 58.587 74.745 1.00 11.55 DIC ATOM 1618 CG ASN 204 39.488 60.025 74.710 1.00 12.55 DIC ATOM 1619 OD1 ASN 204 39.185 60.613 75.752 1.00 15.02 DIC ATOM 1620 ND2 ASN 204 39.418 60.598 73.512 1.00 8.71 DIC ATOM 1621 C ASN 204 37.887 57.647 73.722 1.00 11.96 DIC ATOM 1622 O ASN 204 38.075 56.844 72.803 1.00 10.62 DIC ATOM 1623 N SER 205 36.927 58.566 73.690 1.00 9.54 DIC ATOM 1624 CA SER 205 36.031 58.653 72.550 1.00 11.60 DIC ATOM 1625 CB SER 205 34.888 59.634 72.853 1.00 11.61 DIC ATOM 1626 OG SER 205 33.979 59.055 73.784 1.00 10.36 DIC ATOM 1627 C SER 205 36.718 59.013 71.227 1.00 11.44 DIC ATOM 1628 O SER 205 36.099 58.920 70.166 1.00 11.98 DIC ATOM 1629 N ARG 206 37.994 59.396 71.270 1.00 10.73 DIC ATOM 1630 CA ARG 206 38.686 59.724 70.028 1.00 10.60 DIC ATOM 1631 CB ARG 206 40.089 60.297 70.305 1.00 10.09 DIC ATOM 1632 CG ARG 206 41.089 59.315 70.924 1.00 11.89 DIC ATOM 1633 CD ARG 206 42.374 60.043 71.336 1.00 12.09 DIC ATOM 1634 NE ARG 206 42.939 60.770 70.203 1.00 12.43 DIC ATOM 1635 CZ ARG 206 43.984 60.367 69.484 1.00 10.79 DIC ATOM 1636 NH1 ARG 206 44.610 59.240 69.782 1.00 11.45 DIC ATOM 1637 NH2 ARG 206 44.378 61.078 68.438 1.00 9.92 DIC ATOM 1638 C ARG 206 38.789 58.473 69.149 1.00 9.80 DIC ATOM 1639 O ARG 206 38.932 58.573 67.937 1.00 9.66 DIC ATOM 1640 N PHE 207 38.700 57.295 69.757 1.00 9.55 DIC ATOM 1641 CA PHE 207 38.801 56.056 68.989 1.00 9.03 DIC ATOM 1642 CB PHE 207 39.554 55.009 69.802 1.00 8.47 DIC ATOM 1643 CG PHE 207 40.980 55.386 70.082 1.00 7.54 DIC ATOM 1644 CD1 PHE 207 41.388 55.703 71.368 1.00 7.40 DIC ATOM 1645 CD2 PHE 207 41.906 55.455 69.048 1.00 7.60 DIC ATOM 1646 CE1 PHE 207 42.701 56.087 71.626 1.00 9.11 DIC ATOM 1647 CE2 PHE 207 43.217 55.837 69.290 1.00 10.35 DIC ATOM 1648 CZ PHE 207 43.616 56.156 70.588 1.00 9.62 DIC ATOM 1649 C PHE 207 37.472 55.488 68.495 1.00 9.66 DIC ATOM 1650 O PHE 207 37.416 54.376 67.966 1.00 10.94 DIC ATOM 1651 N ASN 208 36.404 56.254 68.683 1.00 9.27 DIC ATOM 1652 CA ASN 208 35.079 55.866 68.229 1.00 10.30 DIC ATOM 1653 CB ASN 208 34.475 54.792 69.140 1.00 9.11 DIC ATOM 1654 CG ASN 208 33.285 54.091 68.497 1.00 9.58 DIC ATOM 1655 OD1 ASN 208 32.668 54.626 67.573 1.00 9.75 DIC ATOM 1656 ND2 ASN 208 32.956 52.896 68.981 1.00 5.82 DIC ATOM 1657 C ASN 208 34.249 57.144 68.293 1.00 11.23 DIC ATOM 1658 O ASN 208 33.407 57.303 69.172 1.00 11.29 DIC ATOM 1659 N PHE 209 34.514 58.060 67.359 1.00 11.31 DIC ATOM 1660 CA PHE 209 33.835 59.357 67.300 1.00 11.35 DIC ATOM 1661 CB PHE 209 34.800 60.407 66.725 1.00 10.07 DIC ATOM 1662 CG PHE 209 34.402 61.833 67.007 1.00 10.65 DIC ATOM 1663 CD1 PHE 209 34.457 62.348 68.300 1.00 12.23 DIC ATOM 1664 CD2 PHE 209 33.991 62.669 65.972 1.00 12.03 DIC ATOM 1665 CE1 PHE 209 34.110 63.682 68.558 1.00 14.04 DIC ATOM 1666 CE2 PHE 209 33.646 63.991 66.213 1.00 12.22 DIC ATOM 1667 CZ PHE 209 33.705 64.504 67.512 1.00 13.59 DIC ATOM 1668 C PHE 209 32.585 59.241 66.422 1.00 11.70 DIC ATOM 1669 O PHE 209 32.676 59.193 65.198 1.00 10.06 DIC ATOM 1670 N MSE 210 31.419 59.214 67.057 1.00 11.79 DIC ATOM 1671 CA MSE 210 30.156 59.050 66.339 1.00 13.38 DIC ATOM 1672 CB MSE 210 29.343 57.935 67.022 1.00 13.32 DIC ATOM 1673 CG MSE 210 30.087 56.594 67.064 1.00 14.56 DIC ATOM 1674 SE MSE 210 29.331 55.241 68.266 1.00 14.26 DIC ATOM 1675 CE MSE 210 30.349 55.687 69.839 1.00 11.50 DIC ATOM 1676 C MSE 210 29.349 60.344 66.251 1.00 12.91 DIC ATOM 1677 O MSE 210 29.739 61.369 66.815 1.00 11.87 DIC ATOM 1678 N PRO 211 28.225 60.323 65.512 1.00 14.20 DIC ATOM 1679 CD PRO 211 27.659 59.232 64.699 1.00 12.16 DIC ATOM 1680 CA PRO 211 27.406 61.533 65.386 1.00 14.02 DIC ATOM 1681 CB PRO 211 26.159 61.028 64.667 1.00 13.37 DIC ATOM 1682 CG PRO 211 26.719 59.976 63.771 1.00 14.79 DIC ATOM 1683 C PRO 211 27.078 62.175 66.732 1.00 14.59 DIC ATOM 1684 O PRO 211 27.129 63.401 66.873 1.00 14.82 DIC ATOM 1685 N THR 212 26.747 61.356 67.724 1.00 12.84 DIC ATOM 1686 CA THR 212 26.415 61.915 69.026 1.00 12.38 DIC ATOM 1687 CB THR 212 25.861 60.847 69.985 1.00 11.66 DIC ATOM 1688 OG1 THR 212 24.754 60.185 69.367 1.00 10.96 DIC ATOM 1689 CG2 THR 212 25.354 61.505 71.274 1.00 12.45 DIC ATOM 1690 C THR 212 27.614 62.618 69.670 1.00 13.42 DIC ATOM 1691 O THR 212 27.448 63.662 70.307 1.00 12.42 DIC ATOM 1692 N ASN 213 28.813 62.056 69.511 1.00 11.99 DIC ATOM 1693 CA ASN 213 30.016 62.680 70.070 1.00 11.39 DIC ATOM 1694 CB ASN 213 31.268 61.848 69.759 1.00 10.41 DIC ATOM 1695 CG ASN 213 31.210 60.442 70.348 1.00 9.67 DIC ATOM 1696 OD1 ASN 213 31.672 60.196 71.466 1.00 10.66 DIC ATOM 1697 ND2 ASN 213 30.637 59.515 69.595 1.00 7.33 DIC ATOM 1698 C ASN 213 30.155 64.050 69.412 1.00 13.60 DIC ATOM 1699 O ASN 213 30.443 65.045 70.076 1.00 13.49 DIC ATOM 1700 N TYR 214 29.948 64.093 68.097 1.00 13.25 DIC ATOM 1701 CA TYR 214 30.042 65.345 67.358 1.00 16.71 DIC ATOM 1702 CB TYR 214 29.790 65.116 65.863 1.00 17.70 DIC ATOM 1703 CG TYR 214 29.918 66.380 65.041 1.00 21.47 DIC ATOM 1704 CD1 TYR 214 31.165 66.831 64.609 1.00 23.78 DIC ATOM 1705 CE1 TYR 214 31.297 68.018 63.888 1.00 24.82 DIC ATOM 1706 CD2 TYP 214 28.798 67.147 64.732 1.00 24.77 DIC ATOM 1707 CE2 TYR 214 28.915 68.339 64.013 1.00 26.67 DIC ATOM 1708 CZ TYR 214 30.168 68.768 63.594 1.00 27.64 DIC ATOM 1709 OH TYR 214 30.291 69.949 62.885 1.00 28.93 DIC ATOM 1710 C TYR 214 29.014 66.340 67.894 1.00 18.21 DIC ATOM 1711 O TYR 214 29.348 67.483 68.209 1.00 16.24 DIC ATOM 1712 N ALA 215 27.759 65.906 67.985 1.00 18.99 DIC ATOM 1713 CA ALA 215 26.700 66.774 68.488 1.00 21.66 DIC ATOM 1714 CB ALA 215 25.379 66.021 68.547 1.00 19.99 DIC ATOM 1715 C ALA 215 27.096 67.252 69.877 1.00 24.02 DIC ATOM 1716 O ALA 215 26.776 68.374 70.277 1.00 23.13 DIC ATOM 1717 N PHE 216 27.802 66.397 70.609 1.00 26.12 DIC ATOM 1718 CA PHE 216 28.240 66.755 71.945 1.00 31.30 DIC ATOM 1719 CB PHE 216 28.883 65.562 72.648 1.00 32.05 DIC ATOM 1720 CG PHE 216 29.073 65.769 74.123 1.00 34.39 DIC ATOM 1721 CD1 PHE 216 27.973 65.938 74.960 1.00 34.65 DIC ATOM 1722 CD2 PHE 216 30.350 65.808 74.677 1.00 33.95 DIC ATOM 1723 CE1 PHE 216 28.141 66.146 76.328 1.00 34.98 DIC ATOM 1724 CE2 PHE 216 30.528 66.016 76.046 1.00 35.12 DIC ATOM 1725 CZ PHE 216 29.422 66.186 76.871 1.00 34.75 DIC ATOM 1726 C PHE 216 29.237 67.905 71.839 1.00 34.43 DIC ATOM 1727 O PHE 216 29.444 68.639 72.802 1.00 34.68 DIC ATOM 1728 N MSE 217 29.862 68.048 70.670 1.00 37.59 DIC ATOM 1729 CA MSE 217 30.794 69.152 70.445 1.00 40.37 DIC ATOM 1730 CB MSE 217 31.572 68.981 69.134 1.00 42.90 DIC ATOM 1731 CG MSE 217 32.503 67.782 69.051 1.00 46.79 DIC ATOM 1732 SE MSE 217 33.962 67.801 70.312 1.00 54.87 DIC ATOM 1733 CE MSE 217 34.812 69.461 69.818 1.00 51.10 DIC ATOM 1734 C MSE 217 29.898 70.381 70.329 1.00 40.97 DIC ATOM 1735 O MSE 217 29.756 70.961 69.249 1.00 41.56 DIC ATOM 1736 N ALA 218 29.278 70.748 71.446 1.00 41.05 DIC ATOM 1737 CA ALA 218 28.374 71.890 71.526 1.00 40.94 DIC ATOM 1738 CB ALA 218 27.354 71.852 70.384 1.00 40.11 DIC ATOM 1739 C ALA 218 27.662 71.818 72.877 1.00 40.36 DIC ATOM 1740 OT1 ALA 218 26.415 71.718 72.922 1.00 18.66 DIC ATOM 1741 OT2 ALA 218 28.375 71.852 73.894 1.00 18.66 DIC ATOM 1742 CB ALA 222 25.959 69.432 79.985 1.00 40.17 DIC ATOM 1743 C ALA 222 25.843 67.067 79.228 1.00 40.29 DIC ATOM 1744 O ALA 222 24.922 66.318 78.894 1.00 42.05 DIC ATOM 1745 N ALA 222 24.590 68.826 78.056 1.00 38.20 DIC ATOM 1746 CA ALA 222 25.844 68.531 78.798 1.00 39.59 DIC ATOM 1747 N SER 223 26.884 66.669 79.959 1.00 39.44 DIC ATOM 1748 CA SER 223 27.149 65.301 80.439 1.00 38.81 DIC ATOM 1749 CB SER 223 28.411 65.284 81.274 1.00 39.72 DIC ATOM 1750 OG SER 223 28.906 63.978 81.237 1.00 41.10 DIC ATOM 1751 C SER 223 26.135 64.549 81.278 1.00 37.39 DIC ATOM 1752 O SER 223 25.489 65.136 82.124 1.00 36.31 DIC ATOM 1753 N ARG 224 26.103 63.225 81.092 1.00 35.52 DIC ATOM 1754 CA ARG 224 25.222 62.245 81.777 1.00 34.47 DIC ATOM 1755 CB ARG 224 25.124 60.971 80.896 1.00 33.95 DIC ATOM 1756 CG ARG 224 23.749 60.549 80.430 1.00 35.88 DIC ATOM 1757 CD ARG 224 23.144 59.698 81.482 1.00 36.44 DIC ATOM 1758 NE ARG 224 21.699 59.611 81.371 1.00 37.64 DIC ATOM 1759 CZ ARG 224 20.913 59.130 82.315 1.00 38.47 DIC ATOM 1760 NH1 ARG 224 19.608 59.097 82.127 1.00 38.82 DIC ATOM 1761 NH2 ARG 224 21.445 58.665 83.422 1.00 39.33 DIC ATOM 1762 C ARG 224 25.652 61.827 83.196 1.00 32.76 DIC ATOM 1763 O ARG 224 24.831 61.475 84.013 1.00 33.35 DIC ATOM 1764 N HIS 225 26.950 61.845 83.467 1.00 31.17 DIC ATOM 1765 CA HIS 225 27.465 61.469 84.792 1.00 28.74 DIC ATOM 1766 CB HIS 225 28.059 60.055 84.761 1.00 28.53 DIC ATOM 1767 CG HIS 225 27.099 59.000 84.295 1.00 28.65 DIC ATOM 1768 CD2 HIS 225 26.931 58.416 83.083 1.00 28.14 DIC ATOM 1769 ND1 HIS 225 26.140 58.451 85.118 1.00 26.79 DIC ATOM 1770 CE1 HIS 225 25.422 57.576 84.435 1.00 27.52 DIC ATOM 1771 NE2 HIS 225 25.881 57.537 83.197 1.00 27.77 DIC ATOM 1772 C HIS 225 28.535 62.441 85.283 1.00 28.61 DIC ATOM 1773 O HIS 225 29.209 63.061 84.468 1.00 28.11 DIC ATOM 1774 N THR 226 28.700 62.567 86.600 1.00 26.51 DIC ATOM 1775 CA THR 226 29.713 63.466 87.150 1.00 24.55 DIC ATOM 1776 CB THR 226 29.241 64.076 88.488 1.00 24.86 DIC ATOM 1777 OG1 THR 226 28.907 63.025 89.402 1.00 25.94 DIC ATOM 1778 CG2 THR 226 28.010 64.942 88.268 1.00 24.89 DIC ATOM 1779 C THR 226 31.007 62.678 87.360 1.00 23.42 DIC ATOM 1780 O THR 226 32.091 63.247 87.525 1.00 22.81 DIC ATOM 1781 N ASP 227 30.875 61.353 87.352 1.00 21.74 DIC ATOM 1782 CA ASP 227 32.014 60.456 87.515 1.00 20.74 DIC ATOM 1783 CB ASP 227 31.634 59.036 87.073 1.00 20.56 DIC ATOM 1784 CG ASP 227 32.817 58.091 87.067 1.00 20.53 DIC ATOM 1785 OD1 ASP 227 32.691 56.986 86.495 1.00 22.53 DIC ATOM 1786 OD2 ASP 227 33.872 58.442 87.633 1.00 21.73 DIC ATOM 1787 C ASP 227 33.188 60.957 86.672 1.00 20.76 DIC ATOM 1788 O ASP 227 33.118 60.985 85.440 1.00 17.27 DIC ATOM 1789 N PRO 228 34.288 61.351 87.331 1.00 21.29 DIC ATOM 1790 CD PRO 228 34.547 61.210 88.776 1.00 22.76 DIC ATOM 1791 CA PRO 228 35.476 61.853 86.634 1.00 21.24 DIC ATOM 1792 CB PRO 228 36.476 62.076 87.772 1.00 23.32 DIC ATOM 1793 CG PRO 228 36.047 61.074 88.809 1.00 24.69 DIC ATOM 1794 C PRO 228 36.010 60.921 85.549 1.00 21.24 DIC ATOM 1795 O PRO 228 36.503 61.383 84.518 1.00 20.14 DIC ATOM 1796 N LEU 229 35.913 59.612 85.766 1.00 20.48 DIC ATOM 1797 CA LEU 229 36.397 58.677 84.758 1.00 19.34 DIC ATOM 1798 CB LEU 229 36.439 57.257 85.318 1.00 20.42 DIC ATOM 1799 CG LEU 229 36.953 56.172 84.371 1.00 22.18 DIC ATOM 1800 CD1 LEU 229 37.630 55.069 85.167 1.00 22.60 DIC ATOM 1801 CD2 LEU 229 35.792 55.624 83.545 1.00 20.97 DIC ATOM 1802 C LEU 229 35.502 58.739 83.526 1.00 17.99 DIC ATOM 1803 O LEU 229 35.990 58.809 82.397 1.00 17.37 DIC ATOM 1804 N TYR 230 34.192 58.723 83.746 1.00 18.30 DIC ATOM 1805 CA TYR 230 33.234 58.796 82.647 1.00 17.44 DIC ATOM 1806 CB TYR 230 31.799 58.862 83.189 1.00 18.25 DIC ATOM 1807 CG TYR 230 30.741 58.971 82.109 1.00 16.68 DIC ATOM 1808 CD1 TYR 230 30.333 57.850 81.385 1.00 18.08 DIC ATOM 1809 CE1 TYR 230 29.388 57.953 80.370 1.00 16.04 DIC ATOM 1810 CD2 TYR 230 30.173 60.202 81.788 1.00 16.80 DIC ATOM 1811 CE2 TYR 230 29.232 60.320 80.777 1.00 16.57 DIC ATOM 1812 CZ TYR 230 28.842 59.192 80.070 1.00 17.59 DIC ATOM 1813 OH TYR 230 27.908 59.314 79.067 1.00 13.29 DIC ATOM 1814 C TYR 230 33.520 60.049 81.818 1.00 18.05 DIC ATOM 1815 O TYR 230 33.575 59.996 80.588 1.00 17.20 DIC ATOM 1816 N ARG 231 33.704 61.174 82.504 1.00 17.40 DIC ATOM 1817 CA ARG 231 33.979 62.438 81.829 1.00 18.57 DIC ATOM 1818 CB ARG 231 33.948 63.585 82.841 1.00 21.41 DIC ATOM 1819 CG ARG 231 32.535 63.903 83.336 1.00 27.36 DIC ATOM 1820 CD ARG 231 32.562 64.595 84.685 1.00 32.89 DIC ATOM 1821 NE ARG 231 33.446 65.755 84.670 1.00 39.04 DIC ATOM 1822 CZ ARG 231 33.229 66.848 83.946 1.00 41.47 DIC ATOM 1823 NH1 ARG 231 34.092 67.858 83.988 1.00 42.86 DIC ATOM 1824 NH2 ARG 231 32.142 66.936 83.187 1.00 43.95 DIC ATOM 1825 C ARG 231 35.307 62.420 81.079 1.00 18.13 DIC ATOM 1826 O ARG 231 35.407 62.943 79.972 1.00 16.25 DIC ATOM 1827 N ASP 232 36.328 61.821 81.678 1.00 16.04 DIC ATOM 1828 CA ASP 232 37.620 61.749 81.021 1.00 17.65 DIC ATOM 1829 CB ASP 232 38.646 61.092 81.948 1.00 19.41 DIC ATOM 1830 CG ASP 232 39.972 60.839 81.258 1.00 22.20 DIC ATOM 1831 OD1 ASP 232 40.137 59.760 80.648 1.00 24.13 DIC ATOM 1832 OD2 ASP 232 40.845 61.729 81.314 1.00 24.43 DIC ATOM 1833 C ASP 232 37.522 60.957 79.713 1.00 17.38 DIC ATOM 1834 O ASP 232 38.078 61.359 78.690 1.00 16.38 DIC ATOM 1835 N ARG 233 36.789 59.844 79.746 1.00 15.90 DIC ATOM 1836 CA ARG 233 36.647 58.992 78.574 1.00 14.22 DIC ATOM 1837 CB ARG 233 36.134 57.609 78.993 1.00 13.65 DIC ATOM 1838 CG ARG 233 36.992 56.898 80.042 1.00 12.06 DIC ATOM 1839 CD ARG 233 38.359 56.471 79.507 1.00 11.93 DIC ATOM 1840 NE ARG 233 38.994 55.502 80.393 1.00 12.99 DIC ATOM 1841 CZ ARG 233 39.587 55.800 81.549 1.00 18.67 DIC ATOM 1842 NH1 ARG 233 39.647 57.056 81.976 1.00 15.62 DIC ATOM 1843 NH2 ARG 233 40.096 54.829 82.301 1.00 19.37 DIC ATOM 1844 C ARG 233 35.745 59.560 77.477 1.00 14.94 DIC ATOM 1845 O ARG 233 36.042 59.407 76.291 1.00 13.66 DIC ATOM 1846 N THR 234 34.656 60.222 77.867 1.00 14.04 DIC ATOM 1847 CA THR 234 33.716 60.772 76.895 1.00 14.66 DIC ATOM 1848 CB THR 234 32.298 60.886 77.513 1.00 15.37 DIC ATOM 1849 OG1 TSP 234 32.365 61.614 78.745 1.00 12.97 DIC ATOM 1850 CG2 THR 234 31.725 59.474 77.789 1.00 14.09 DIC ATOM 1851 C THR 234 34.149 62.114 76.298 1.00 16.57 DIC ATOM 1852 O THR 234 33.618 62.555 75.282 1.00 15.27 DIC ATOM 1853 N ASN 235 35.115 62.767 76.926 1.00 16.09 DIC ATOM 1854 CA ASN 235 35.594 64.017 76.386 1.00 18.20 DIC ATOM 1855 CB ASN 235 36.034 64.941 77.519 1.00 22.89 DIC ATOM 1856 CG ASN 235 34.843 65.640 78.171 1.00 28.06 DIC ATOM 1857 OD1 ASN 235 34.410 66.700 77.716 1.00 32.63 DIC ATOM 1858 ND2 ASN 235 34.282 65.029 79.210 1.00 30.92 DIC ATOM 1859 C ASN 235 36.708 63.648 75.423 1.00 17.06 DIC ATOM 1860 O ASN 235 37.793 63.214 75.810 1.00 14.88 DIC ATOM 1861 N THR 236 36.389 63.780 74.142 1.00 16.31 DIC ATOM 1862 CA THR 236 37.308 63.421 73.084 1.00 14.87 DIC ATOM 1863 CB THR 236 36.623 63.547 71.714 1.00 15.58 DIC ATOM 1864 OG1 THR 236 35.566 62.578 71.629 1.00 14.42 DIC ATOM 1865 CG2 THR 236 37.619 63.309 70.588 1.00 13.74 DIC ATOM 1866 C THR 236 38.587 64.219 73.088 1.00 15.17 DIC ATOM 1867 O THR 236 38.567 65.454 73.120 1.00 15.92 DIC ATOM 1868 N VAL 237 39.706 63.503 73.086 1.00 13.08 DIC ATOM 1869 CA VAL 237 41.006 64.150 73.049 1.00 14.84 DIC ATOM 1870 CB VAL 237 42.080 63.350 73.818 1.00 16.34 DIC ATOM 1871 CG1 VAL 237 43.444 64.022 73.635 1.00 16.24 DIC ATOM 1872 CG2 VAL 237 41.723 63.279 75.308 1.00 16.15 DIC ATOM 1873 C VAL 237 41.388 64.205 71.574 1.00 14.29 DIC ATOM 1874 O VAL 237 41.667 63.174 70.954 1.00 13.91 DIC ATOM 1875 N MSE 238 41.380 65.408 71.015 1.00 14.48 DIC ATOM 1876 CA MSE 238 41.710 65.608 69.603 1.00 15.10 DIC ATOM 1877 CB MSE 238 41.462 67.065 69.223 1.00 16.28 DIC ATOM 1878 CG MSE 238 40.012 67.495 69.341 1.00 20.30 DIC ATOM 1879 SE MSE 238 38.859 66.527 68.131 1.00 22.47 DIC ATOM 1880 CE MSE 238 37.180 66.780 69.061 1.00 25.99 DIC ATOM 1881 C MSE 238 43.160 65.234 69.288 1.00 13.91 DIC ATOM 1882 O MSE 238 44.021 65.289 70.163 1.00 14.24 DIC ATOM 1883 N PRO 239 43.451 64.872 68.022 1.00 14.10 DIC ATOM 1884 CD PRO 239 44.832 64.616 67.570 1.00 14.78 DIC ATOM 1885 CA PRO 239 42.515 64.788 66.895 1.00 13.37 DIC ATOM 1886 CB PRO 239 43.438 64.848 65.682 1.00 14.16 DIC ATOM 1887 CG PRO 239 44.630 64.088 66.154 1.00 15.87 DIC ATOM 1888 C PRO 239 41.696 63.501 66.914 1.00 13.85 DIC ATOM 1889 O PRO 239 42.065 62.530 67.582 1.00 12.56 DIC ATOM 1890 N VAL 240 40.588 63.490 66.179 1.00 12.87 DIC ATOM 1891 CA VAL 240 39.758 62.296 66.118 1.00 12.68 DIC ATOM 1892 CB VAL 240 38.485 62.538 65.260 1.00 13.59 DIC ATOM 1893 CG1 VAL 240 37.735 61.231 65.054 1.00 15.84 DIC ATOM 1894 CG2 VAL 240 37.574 63.557 65.962 1.00 13.32 DIC ATOM 1895 C VAL 240 40.615 61.210 65.494 1.00 11.91 DIC ATOM 1896 O VAL 240 41.331 61.470 64.526 1.00 12.36 DIC ATOM 1897 N ALA 241 40.566 60.003 66.054 1.00 10.60 DIC ATOM 1898 CA ALA 241 41.366 58.887 65.529 1.00 9.24 DIC ATOM 1899 CB ALA 241 41.989 58.107 66.688 1.00 8.43 DIC ATOM 1900 C ALA 241 40.515 57.960 64.663 1.00 9.78 DIC ATOM 1901 O ALA 241 40.990 57.400 63.673 1.00 9.54 DIC ATOM 1902 N VAL 242 39.250 57.804 65.042 1.00 8.78 DIC ATOM 1903 CA VAL 242 38.327 56.961 64.296 1.00 8.01 DIC ATOM 1904 CB VAL 242 38.120 55.590 64.998 1.00 8.78 DIC ATOM 1905 CG1 VAL 242 37.181 54.717 64.170 1.00 7.09 DIC ATOM 1906 CG2 VAL 242 39.458 54.896 65.195 1.00 7.39 DIC ATOM 1907 C VAL 242 36.955 57.604 64.163 1.00 9.79 DIC ATOM 1908 O VAL 242 36.311 57.906 65.170 1.00 9.84 DIC ATOM 1909 N SER 243 36.521 57.830 62.924 1.00 10.04 DIC ATOM 1910 CA SER 243 35.194 58.371 62.658 1.00 11.61 DIC ATOM 1911 CB SER 243 35.153 59.147 61.331 1.00 12.32 DIC ATOM 1912 OG SER 243 35.555 60.495 61.486 1.00 16.91 DIC ATOM 1913 C SER 243 34.344 57.115 62.509 1.00 12.31 DIC ATOM 1914 O SER 243 34.747 56.183 61.820 1.00 13.73 DIC ATOM 1915 N HIS 244 33.189 57.078 63.165 1.00 11.25 DIC ATOM 1916 CA HIS 244 32.297 55.925 63.079 1.00 9.29 DIC ATOM 1917 CB HIS 244 32.266 55.187 64.429 1.00 7.53 DIC ATOM 1918 CG HIS 244 31.407 53.958 64.434 1.00 8.43 DIC ATOM 1919 CD2 HIS 244 30.813 53.278 63.424 1.00 7.51 DIC ATOM 1920 ND1 HIS 244 31.055 53.302 65.598 1.00 6.41 DIC ATOM 1921 CE1 HIS 244 30.277 52.274 65.300 1.00 8.12 DIC ATOM 1922 NE2 HIS 244 30.114 52.238 63.990 1.00 6.81 DIC ATOM 1923 C HIS 244 30.903 56.446 62.710 1.00 9.33 DIC ATOM 1924 O HIS 244 30.278 57.173 63.477 1.00 9.05 DIC ATOM 1925 N TYR 245 30.423 56.073 61.530 1.00 9.10 DIC ATOM 1926 CA TYR 245 29.120 56.524 61.051 1.00 10.38 DIC ATOM 1927 CB TYR 245 29.213 56.762 59.545 1.00 11.80 DIC ATOM 1928 CG TYR 245 30.308 57.747 59.216 1.00 13.82 DIC ATOM 1929 CD1 TYR 245 30.092 59.118 59.344 1.00 14.45 DIC ATOM 1930 CE1 TYR 245 31.127 60.035 59.150 1.00 16.51 DIC ATOM 1931 CD2 TYR 245 31.591 57.308 58.875 1.00 14.05 DIC ATOM 1932 CE2 TYR 245 32.636 58.217 58.679 1.00 15.80 DIC ATOM 1933 CZ TYR 245 32.396 59.579 58.822 1.00 16.33 DIC ATOM 1934 OH TYR 245 33.422 60.487 58.666 1.00 15.53 DIC ATOM 1935 C TYR 245 27.991 55.552 61.380 1.00 11.30 DIC ATOM 1936 O TYR 245 27.281 55.062 60.490 1.00 10.36 DIC ATOM 1937 N CYS 246 27.818 55.284 62.670 1.00 11.34 DIC ATOM 1938 CA CYS 246 26.781 54.363 63.101 1.00 13.80 DIC ATOM 1939 CB CYS 246 26.886 54.103 64.605 1.00 15.97 DIC ATOM 1940 SG CYS 246 26.808 55.590 65.610 1.00 19.68 DIC ATOM 1941 C CYS 246 25.422 54.947 62.763 1.00 15.08 DIC ATOM 1942 O CYS 246 25.254 56.167 62.704 1.00 14.66 DIC ATOM 1943 N GLY 247 24.453 54.071 62.529 1.00 14.33 DIC ATOM 1944 CA GLY 247 23.127 54.539 62.191 1.00 14.42 DIC ATOM 1945 C GLY 247 22.893 54.396 60.703 1.00 16.40 DIC ATOM 1946 O GLY 247 23.789 53.977 59.974 1.00 14.60 DIC ATOM 1947 N PRO 248 21.693 54.754 60.218 1.00 17.44 DIC ATOM 1948 CD PRO 248 20.586 55.331 61.001 1.00 17.20 DIC ATOM 1949 CA PRO 248 21.334 54.660 58.800 1.00 17.61 DIC ATOM 1950 CB PRO 248 19.845 55.009 58.809 1.00 19.08 DIC ATOM 1951 CG PRO 248 19.750 56.000 59.933 1.00 18.65 DIC ATOM 1952 C PRO 248 22.132 55.545 57.833 1.00 17.78 DIC ATOM 1953 O PRO 248 22.311 55.187 56.675 1.00 18.06 DIC ATOM 1954 N ALA 249 22.617 56.690 58.305 1.00 18.95 DIC ATOM 1955 CA ALA 249 23.362 57.612 57.444 1.00 18.77 DIC ATOM 1956 CB ALA 249 23.276 59.038 58.008 1.00 18.55 DIC ATOM 1957 C ALA 249 24.823 57.206 57.266 1.00 18.31 DIC ATOM 1958 O ALA 249 25.635 57.356 58.178 1.00 19.11 DIC ATOM 1959 N LYS 250 25.156 56.705 56.082 1.00 16.06 DIC ATOM 1960 CA LYS 250 26.515 56.269 55.808 1.00 16.76 DIC ATOM 1961 CB LYS 250 26.498 54.854 55.226 1.00 14.84 DIC ATOM 1962 CG LYS 250 25.771 53.836 56.093 1.00 14.31 DIC ATOM 1963 CD LYS 250 26.384 53.731 57.487 1.00 14.00 DIC ATOM 1964 CE LYS 250 25.797 52.551 58.272 1.00 11.62 DIC ATOM 1965 NZ LYS 250 26.190 52.604 59.721 1.00 9.99 DIC ATOM 1966 C LYS 250 27.246 57.213 54.857 1.00 17.98 DIC ATOM 1967 O LYS 250 26.621 57.890 54.036 1.00 17.45 DIC ATOM 1968 N PRO 251 28.588 57.251 54.943 1.00 18.59 DIC ATOM 1969 CD PRO 251 29.466 56.428 55.797 1.00 19.31 DIC ATOM 1970 CA PRO 251 29.379 58.126 54.076 1.00 19.82 DIC ATOM 1971 CB PRO 251 30.792 57.983 54.640 1.00 18.90 DIC ATOM 1972 CG PRO 251 30.815 56.562 55.106 1.00 19.40 DIC ATOM 1973 C PRO 251 29.278 57.761 52.594 1.00 21.72 DIC ATOM 1974 O PRO 251 29.544 58.602 51.731 1.00 22.19 DIC ATOM 1975 N TRP 252 28.885 56.521 52.298 1.00 22.68 DIC ATOM 1976 CA TRP 252 28.732 56.090 50.904 1.00 24.72 DIC ATOM 1977 CB TRP 252 29.053 54.599 50.751 1.00 22.37 DIC ATOM 1978 CG TRP 252 28.332 53.709 51.710 1.00 17.98 DIC ATOM 1979 CD2 TRP 252 28.886 53.095 52.875 1.00 16.74 DIC ATOM 1980 CE2 TRP 252 27.856 52.345 53.485 1.00 15.49 DIC ATOM 1981 CE3 TRP 252 30.156 53.105 53.466 1.00 14.56 DIC ATOM 1982 CD1 TRP 252 27.022 53.321 51.658 1.00 18.51 DIC ATOM 1983 NE1 TRP 252 26.728 52.500 52.722 1.00 15.35 DIC ATOM 1984 CZ2 TRP 252 28.058 51.613 54.657 1.00 15.42 DIC ATOM 1985 CZ3 TRP 252 30.356 52.378 54.630 1.00 14.20 DIC ATOM 1986 CH2 TRP 252 29.312 51.642 55.212 1.00 14.24 DIC ATOM 1987 C TRP 252 27.318 56.372 50.397 1.00 27.39 DIC ATOM 1988 O TRP 252 26.969 56.026 49.266 1.00 28.26 DIC ATOM 1989 N HIS 253 26.512 56.996 51.249 1.00 30.21 DIC ATOM 1990 CA HIS 253 25.140 57.358 50.909 1.00 34.07 DIC ATOM 1991 CB HIS 253 24.228 57.315 52.138 1.00 34.17 DIC ATOM 1992 CG HIS 253 23.745 55.947 52.498 1.00 34.88 DIC ATOM 1993 CD2 HIS 253 23.210 55.469 53.644 1.00 34.49 DIC ATOM 1994 ND1 HIS 253 23.731 54.903 51.598 1.00 33.80 DIC ATOM 1995 CE1 HIS 253 23.206 53.837 52.178 1.00 35.02 DIC ATOM 1996 NE2 HIS 253 22.881 54.152 53.419 1.00 35.95 DIC ATOM 1997 C HIS 253 25.102 58.778 50.364 1.00 36.66 DIC ATOM 1998 O HIS 253 26.079 59.525 50.464 1.00 37.76 DIC ATOM 1999 N ARG 254 23.954 59.144 49.803 1.00 38.76 DIC ATOM 2000 CA ARG 254 23.751 60.476 49.253 1.00 40.22 DIC ATOM 2001 CB ARG 254 22.605 60.449 48.238 1.00 41.70 DIC ATOM 2002 CG ARG 254 22.678 59.273 47.266 1.00 43.79 DIC ATOM 2003 CD ARG 254 21.435 59.178 46.392 1.00 44.39 DIC ATOM 2004 NE ARG 254 20.205 59.068 47.174 1.00 44.17 DIC ATOM 2005 CZ ARG 254 18.991 58.970 46.642 1.00 43.46 DIC ATOM 2006 NH1 ARG 254 18.844 58.969 45.323 1.00 43.96 DIC ATOM 2007 NH2 ARG 254 17.925 58.873 47.425 1.00 42.76 DIC ATOM 2008 C ARG 254 23.392 61.401 50.411 1.00 40.54 DIC ATOM 2009 O ARG 254 22.796 60.969 51.401 1.00 40.03 DIC ATOM 2010 N ASP 255 23.772 62.667 50.291 1.00 40.92 DIC ATOM 2011 CA ASP 255 23.477 63.659 51.315 1.00 41.47 DIC ATOM 2012 CB ASP 255 21.981 63.995 51.280 1.00 42.69 DIC ATOM 2013 CG ASP 255 21.555 64.612 49.953 1.00 43.75 DIC ATOM 2014 OD1 ASP 255 21.950 65.766 49.678 1.00 43.58 DIC ATOM 2015 OD2 ASP 255 20.835 63.939 49.181 1.00 44.62 DIC ATOM 2016 C ASP 255 23.894 63.273 52.738 1.00 41.91 DIC ATOM 2017 O ASP 255 23.144 63.491 53.694 1.00 41.85 DIC ATOM 2018 N CYS 256 25.086 62.696 52.882 1.00 41.35 DIC ATOM 2019 CA CYS 256 25.574 62.338 54.211 1.00 39.96 DIC ATOM 2020 CB CYS 256 26.664 61.266 54.133 1.00 39.72 DIC ATOM 2021 SG CYS 256 27.207 60.674 55.763 1.00 40.45 DIC ATOM 2022 C CYS 256 26.150 63.623 54.800 1.00 38.56 DIC ATOM 2023 O CYS 256 27.114 64.177 54.273 1.00 37.54 DIC ATOM 2024 N THR 257 25.547 64.103 55.883 1.00 38.47 DIC ATOM 2025 CA THR 257 25.996 65.339 56.515 1.00 36.95 DIC ATOM 2026 CB THR 257 24.795 66.183 56.963 1.00 37.26 DIC ATOM 2027 OG1 THR 257 24.065 65.475 57.974 1.00 37.57 DIC ATOM 2028 CG2 THR 257 23.875 66.459 55.780 1.00 36.79 DIC ATOM 2029 C THR 257 26.900 65.089 57.717 1.00 35.26 DIC ATOM 2030 O THR 257 27.333 66.027 58.384 1.00 35.00 DIC ATOM 2031 N ALA 258 27.178 63.820 57.994 1.00 33.98 DIC ATOM 2032 CA ALA 258 28.038 63.457 59.111 1.00 32.05 DIC ATOM 2033 CB ALA 258 28.131 61.943 59.231 1.00 31.18 DIC ATOM 2034 C ALA 258 29.421 64.052 58.889 1.00 31.39 DIC ATOM 2035 O ALA 258 29.867 64.220 57.751 1.00 30.13 DIC ATOM 2036 N TRP 259 30.098 64.362 59.986 1.00 31.29 DIC ATOM 2037 CA TRP 259 31.429 64.955 59.937 1.00 29.92 DIC ATOM 2038 CB TRP 259 31.868 65.341 61.351 1.00 31.14 DIC ATOM 2039 CG TRP 259 33.230 65.947 61.400 1.00 31.00 DIC ATOM 2040 CD2 TRP 259 34.439 65.294 61.798 1.00 30.73 DIC ATOM 2041 CE2 TRP 259 35.484 66.235 61.668 1.00 30.83 DIC ATOM 2042 CE3 TRP 259 34.741 64.004 62.253 1.00 29.98 DIC ATOM 2043 CD1 TRP 259 33.576 67.221 61.053 1.00 30.91 DIC ATOM 2044 NE1 TRP 259 34.930 67.402 61.211 1.00 31.95 DIC ATOM 2045 CZ2 TRP 259 36.811 65.928 61.978 1.00 30.08 DIC ATOM 2046 CZ3 TRP 259 36.058 63.698 62.560 1.00 29.09 DIC ATOM 2047 CH2 TRP 259 37.077 64.657 62.422 1.00 30.00 DIC ATOM 2048 C TRP 259 32.486 64.043 59.313 1.00 29.26 DIC ATOM 2049 O TRP 259 32.509 62.831 59.558 1.00 27.60 DIC ATOM 2050 N GLY 260 33.360 64.645 58.508 1.00 27.51 DIC ATOM 2051 CA GLY 260 34.436 63.912 57.861 1.00 26.27 DIC ATOM 2052 C GLY 260 34.050 62.911 56.788 1.00 26.05 DIC ATOM 2053 O GLY 260 34.909 62.189 56.281 1.00 25.46 DIC ATOM 2054 N ALA 261 32.772 62.862 56.431 1.00 25.27 DIC ATOM 2055 CA ALA 261 32.307 61.922 55.417 1.00 25.33 DIC ATOM 2056 CB ALA 261 30.805 62.112 55.182 1.00 25.36 DIC ATOM 2057 C ALA 261 33.066 62.078 54.101 1.00 25.94 DIC ATOM 2058 O ALA 261 33.265 61.106 53.373 1.00 26.13 DIC ATOM 2059 N ALA 262 33.497 63.300 53.804 1.00 25.58 DIC ATOM 2060 CA ALA 262 34.215 63.585 52.564 1.00 26.27 DIC ATOM 2061 CB ALA 262 34.544 65.078 52.476 1.00 26.51 DIC ATOM 2062 C ALA 262 35.482 62.762 52.350 1.00 26.63 DIC ATOM 2063 O ALA 262 35.900 62.566 51.205 1.00 26.59 DIC ATOM 2064 N ARG 263 36.109 62.275 53.418 1.00 25.79 DIC ATOM 2065 CA ARG 263 37.310 61.487 53.194 1.00 25.44 DIC ATOM 2066 CB ARG 263 38.201 61.364 54.435 1.00 28.92 DIC ATOM 2067 CG ARG 263 39.579 60.821 54.018 1.00 33.60 DIC ATOM 2068 CD ARG 263 40.483 60.390 55.155 1.00 37.93 DIC ATOM 2069 NE ARG 263 41.350 61.455 55.663 1.00 40.10 DIC ATOM 2070 CZ ARG 263 40.995 62.342 56.588 1.00 41.46 DIC ATOM 2071 NH1 ARG 263 41.856 63.267 56.987 1.00 41.19 DIC ATOM 2072 NH2 ARG 263 39.780 62.304 57.116 1.00 43.96 DIC ATOM 2073 C ARG 263 36.988 60.092 52.687 1.00 22.70 DIC ATOM 2074 O ARG 263 37.883 59.374 52.248 1.00 20.54 DIC ATOM 2075 N PHE 264 35.722 59.691 52.757 1.00 20.27 DIC ATOM 2076 CA PHE 264 35.354 58.373 52.245 1.00 19.95 DIC ATOM 2077 CB PHE 264 33.894 58.031 52.559 1.00 19.65 DIC ATOM 2078 CG PHE 264 33.433 56.738 51.934 1.00 18.28 DIC ATOM 2079 CD1 PHE 264 33.634 55.522 52.582 1.00 17.29 DIC ATOM 2080 CD2 PHE 264 32.835 56.734 50.674 1.00 18.28 DIC ATOM 2081 CE1 PHE 264 33.248 54.321 51.986 1.00 18.07 DIC ATOM 2082 CE2 PHE 264 32.446 55.534 50.069 1.00 17.91 DIC ATOM 2083 CZ PHE 264 32.654 54.328 50.729 1.00 17.29 DIC ATOM 2084 C PHE 264 35.526 58.425 50.728 1.00 19.57 DIC ATOM 2085 O PHE 264 36.140 57.548 50.126 1.00 18.73 DIC ATOM 2086 N THR 265 34.976 59.474 50.124 1.00 20.91 DIC ATOM 2087 CA THR 265 35.045 59.665 48.680 1.00 22.89 DIC ATOM 2088 CB THR 265 34.289 60.932 48.252 1.00 24.07 DIC ATOM 2089 OG1 THR 265 32.974 60.922 48.820 1.00 27.93 DIC ATOM 2090 CG2 THR 265 34.179 60.989 46.734 1.00 25.93 DIC ATOM 2091 C THR 265 36.496 59.810 48.252 1.00 23.30 DIC ATOM 2092 O THR 265 36.932 59.238 47.251 1.00 23.08 DIC ATOM 2093 N GLU 266 37.243 60.583 49.026 1.00 23.53 DIC ATOM 2094 CA GLU 266 38.646 60.804 48.733 1.00 25.20 DIC ATOM 2095 CB GLU 266 39.256 61.723 49.784 1.00 28.98 DIC ATOM 2096 CG GLU 266 40.736 61.936 49.607 1.00 36.19 DIC ATOM 2097 CD GLU 266 41.240 63.096 50.427 1.00 39.75 DIC ATOM 2098 OE1 GLU 266 40.976 63.113 51.650 1.00 41.33 DIC ATOM 2099 OE2 GLU 266 41.896 63.991 49.846 1.00 42.17 DIC ATOM 2100 C GLU 266 39.408 59.482 48.687 1.00 23.71 DIC ATOM 2101 O GLU 266 40.195 59.251 47.778 1.00 22.46 DIC ATOM 2102 N LEU 267 39.173 58.616 49.670 1.00 22.23 DIC ATOM 2103 CA LEU 267 39.842 57.320 49.701 1.00 21.24 DIC ATOM 2104 CB LEU 267 39.601 56.617 51.044 1.00 21.75 DIC ATOM 2105 CG LEU 267 40.509 57.054 52.195 1.00 22.58 DIC ATOM 2106 CD1 LEU 267 39.979 56.545 53.520 1.00 23.20 DIC ATOM 2107 CD2 LEU 267 41.918 56.531 51.938 1.00 24.01 DIC ATOM 2108 C LEU 267 39.346 56.443 48.562 1.00 19.60 DIC ATOM 2109 O LEU 267 40.137 55.786 47.888 1.00 19.14 DIC ATOM 2110 N ALA 268 38.035 56.436 48.340 1.00 19.54 DIC ATOM 2111 CA ALA 268 37.458 55.630 47.271 1.00 21.17 DIC ATOM 2112 CB ALA 268 35.949 55.838 47.209 1.00 22.40 DIC ATOM 2113 C ALA 266 38.091 55.999 45.933 1.00 23.39 DIC ATOM 2114 O ALA 268 38.382 55.127 45.108 1.00 23.18 DIC ATOM 2115 N GLY 269 38.306 57.295 45.727 1.00 23.42 DIC ATOM 2116 CA GLY 269 38.896 57.759 44.486 1.00 25.69 DIC ATOM 2117 C GLY 269 40.364 57.408 44.346 1.00 27.18 DIC ATOM 2118 O GLY 269 40.919 57.479 43.249 1.00 27.61 DIC ATOM 2119 N SER 270 40.995 57.029 45.452 1.00 27.80 DIC ATOM 2120 CA SER 270 42.409 56.670 45.438 1.00 28.87 DIC ATOM 2121 CB SER 270 43.065 57.070 46.757 1.00 29.06 DIC ATOM 2122 OG SER 270 42.560 56.279 47.818 1.00 31.44 DIC ATOM 2123 C SER 270 42.616 55.174 45.221 1.00 28.53 DIC ATOM 2124 O SER 270 43.750 54.704 45.156 1.00 28.86 DIC ATOM 2125 N LEU 271 41.525 54.425 45.105 1.00 27.87 DIC ATOM 2126 CA LEU 271 41.633 52.981 44.925 1.00 28.38 DIC ATOM 2127 CB LEU 271 40.240 52.337 44.928 1.00 26.77 DIC ATOM 2128 CG LEU 271 39.478 52.415 46.256 1.00 25.46 DIC ATOM 2129 CD1 LEU 271 38.123 51.727 46.125 1.00 24.92 DIC ATOM 2130 CD2 LEU 271 40.310 51.757 47.348 1.00 24.78 DIC ATOM 2131 C LEU 271 42.383 52.579 43.658 1.00 29.08 DIC ATOM 2132 O LEU 271 42.146 53.122 42.583 1.00 27.21 DIC ATOM 2133 N THR 272 43.288 51.616 43.804 1.00 29.70 DIC ATOM 2134 CA THR 272 44.075 51.115 42.687 1.00 30.05 DIC ATOM 2135 CB THR 272 45.091 50.055 43.158 1.00 30.32 DIC ATOM 2136 OG1 THR 272 45.943 50.617 44.164 1.00 32.13 DIC ATOM 2137 CG2 THR 272 45.935 49.578 41.996 1.00 32.54 DIC ATOM 2138 C THR 272 43.159 50.471 41.649 1.00 29.64 DIC ATOM 2139 O THR 272 43.195 50.830 40.471 1.00 29.15 DIC ATOM 2140 N THR 273 42.344 49.520 42.103 1.00 28.68 DIC ATOM 2141 CA THR 273 41.418 48.803 41.236 1.00 28.77 DIC ATOM 2142 CB THR 273 41.707 47.281 41.225 1.00 31.01 DIC ATOM 2143 OG1 THR 273 43.095 47.050 40.955 1.00 33.16 DIC ATOM 2144 CG2 THR 273 40.868 46.593 40.153 1.00 33.04 DIC ATOM 2145 C THR 273 39.967 48.984 41.675 1.00 26.88 DIC ATOM 2146 O THR 273 39.642 48.858 42.854 1.00 25.29 DIC ATOM 2147 N VAL 274 39.095 49.273 40.717 1.00 24.92 DIC ATOM 2148 CA VAL 274 37.683 49.449 41.025 1.00 23.86 DIC ATOM 2149 CB VAL 274 37.276 50.932 41.006 1.00 23.31 DIC ATOM 2150 CG1 VAL 274 35.839 51.070 41.469 1.00 23.87 DIC ATOM 2151 CG2 VAL 274 38.191 51.737 41.906 1.00 24.43 DIC ATOM 2152 C VAL 274 36.819 48.700 40.019 1.00 23.07 DIC ATOM 2153 O VAL 274 36.593 49.176 38.902 1.00 23.08 DIC ATOM 2154 N PRO 275 36.330 47.510 40.400 1.00 21.69 DIC ATOM 2155 CD PRO 275 36.566 46.776 41.654 1.00 20.50 DIC ATOM 2156 CA PRO 275 35.488 46.726 39.497 1.00 21.63 DIC ATOM 2157 CB PRO 275 35.088 45.524 40.352 1.00 21.49 DIC ATOM 2158 CG PRO 275 36.254 45.356 41.253 1.00 21.48 DIC ATOM 2159 C PRO 275 34.273 47.522 39.048 1.00 21.99 DIC ATOM 2160 O PRO 275 33.736 48.338 39.805 1.00 21.78 DIC ATOM 2161 N GLU 276 33.852 47.284 37.810 1.00 23.31 DIC ATOM 2162 CA GLU 276 32.683 47.943 37.249 1.00 23.31 DIC ATOM 2163 CB GLU 276 32.297 47.256 35.934 1.00 23.72 DIC ATOM 2164 CG GLU 276 30.950 47.667 35.362 1.00 26.81 DIC ATOM 2165 CD GLU 276 30.875 49.144 35.067 1.00 27.36 DIC ATOM 2166 OE1 GLU 276 31.941 49.794 35.028 1.00 31.05 DIC ATOM 2167 OE2 GLU 276 29.755 49.656 34.868 1.00 29.72 DIC ATOM 2168 C GLU 276 31.525 47.846 38.244 1.00 23.02 DIC ATOM 2169 O GLU 276 30.797 48.811 38.473 1.00 23.54 DIC ATOM 2170 N GLU 277 31.376 46.678 38.854 1.00 23.75 DIC ATOM 2171 CA GLU 277 30.294 46.464 39.804 1.00 25.40 DIC ATOM 2172 CB GLU 277 30.168 44.970 40.120 1.00 29.16 DIC ATOM 2173 CG GLU 277 28.715 44.493 40.230 1.00 35.80 DIC ATOM 2174 CD GLU 277 28.022 44.308 38.873 1.00 37.33 DIC ATOM 2175 OE1 GLU 277 28.104 45.210 38.005 1.00 38.08 DIC ATOM 2176 OE2 GLU 277 27.378 43.251 38.685 1.00 39.35 DIC ATOM 2177 C GLU 277 30.407 47.275 41.104 1.00 24.54 DIC ATOM 2178 O GLU 277 29.484 47.275 41.914 1.00 23.39 DIC ATOM 2179 N TRP 278 31.531 47.962 41.300 1.00 23.06 DIC ATOM 2180 CA TRP 278 31.732 48.795 42.489 1.00 20.91 DIC ATOM 2181 CB TRP 278 33.181 48.700 42.986 1.00 18.69 DIC ATOM 2182 CG TRP 278 33.521 47.467 43.781 1.00 17.97 DIC ATOM 2183 CD2 TRP 278 34.676 47.279 44.613 1.00 16.79 DIC ATOM 2184 CE2 TRP 278 34.610 45.970 45.130 1.00 15.02 DIC ATOM 2185 CE3 TRP 278 35.763 48.095 44.970 1.00 16.53 DIC ATOM 2186 CD1 TRP 278 32.822 46.294 43.828 1.00 16.18 DIC ATOM 2187 NE1 TRP 278 33.470 45.390 44.636 1.00 16.36 DIC ATOM 2188 CZ2 TRP 278 35.589 45.450 45.989 1.00 14.14 DIC ATOM 2189 CZ3 TRP 278 36.742 47.577 45.828 1.00 14.30 DIC ATOM 2190 CH2 TRP 278 36.644 46.268 46.324 1.00 13.79 DIC ATOM 2191 C TRP 278 31.441 50.258 42.152 1.00 21.28 DIC ATOM 2192 O TRP 278 31.315 51.093 43.046 1.00 20.17 DIC ATOM 2193 N ALA 279 31.344 50.563 40.860 1.00 22.70 DIC ATOM 2194 CA ALA 279 31.102 51.935 40.412 1.00 24.93 DIC ATOM 2195 CB ALA 279 30.915 51.972 38.899 1.00 27.07 DIC ATOM 2196 C ALA 279 29.903 52.563 41.098 1.00 25.99 DIC ATOM 2197 O ALA 279 29.976 53.690 41.590 1.00 25.88 DIC ATOM 2198 N GLY 280 28.795 51.834 41.134 1.00 27.56 DIC ATOM 2199 CA GLY 280 27.608 52.372 41.772 1.00 30.18 DIC ATOM 2200 C GLY 280 27.801 52.629 43.257 1.00 31.52 DIC ATOM 2201 O GLY 280 27.427 53.680 43.776 1.00 32.79 DIC ATOM 2202 N LYS 281 28.413 51.668 43.937 1.00 31.54 DIC ATOM 2203 CA LYS 281 28.656 51.766 45.370 1.00 32.16 DIC ATOM 2204 CB LYS 281 29.079 50.396 45.911 1.00 31.67 DIC ATOM 2205 CG LYS 281 27.951 49.386 46.055 1.00 33.55 DIC ATOM 2206 CD LYS 281 28.490 48.084 46.637 1.00 34.90 DIC ATOM 2207 CE LYS 281 27.450 47.351 47.477 1.00 36.99 DIC ATOM 2208 NZ LYS 281 26.693 46.315 46.724 1.00 38.19 DIC ATOM 2209 C LYS 281 29.664 52.815 45.826 1.00 32.48 DIC ATOM 2210 O LYS 281 29.484 53.440 46.867 1.00 32.45 DIC ATOM 2211 N LEU 282 30.717 53.007 45.044 1.00 31.92 DIC ATOM 2212 CA LEU 282 31.758 53.953 45.403 1.00 33.81 DIC ATOM 2213 CB LEU 282 33.121 53.402 44.968 1.00 32.92 DIC ATOM 2214 CG LEU 282 34.051 52.818 46.044 1.00 34.56 DIC ATOM 2215 CD1 LEU 282 33.283 52.458 47.313 1.00 32.48 DIC ATOM 2216 CD2 LEU 282 34.752 51.605 45.466 1.00 32.62 DIC ATOM 2217 C LEU 282 31.599 55.383 44.893 1.00 35.67 DIC ATOM 2218 O LEU 282 32.284 56.281 45.373 1.00 37.01 DIC ATOM 2219 N ALA 283 30.711 55.605 43.932 1.00 37.96 DIC ATOM 2220 CA ALA 283 30.501 56.944 43.381 1.00 40.04 DIC ATOM 2221 CB ALA 283 30.102 57.925 44.489 1.00 39.26 DIC ATOM 2222 C ALA 283 31.718 57.476 42.611 1.00 41.65 DIC ATOM 2223 OT1 ALA 283 31.501 57.913 41.458 1.00 43.46 DIC ATOM 2224 OT2 ALA 283 32.858 57.460 43.139 1.00 41.61 DIC ATOM 2225 MN MN 400 29.002 50.705 62.676 1.00 11.41 ATOM 2226 C1 LAT 1347 21.881 53.893 65.661 1.00 28.17 ATOM 2227 C2 LAT 1347 22.143 52.528 65.080 1.00 26.76 ATOM 2228 C3 LAT 1347 22.196 51.524 66.241 1.00 26.19 ATOM 2229 C4 LAT 1347 23.382 51.940 67.197 1.00 25.62 ATOM 2230 C5 LAT 1347 23.232 53.243 67.815 1.00 25.09 ATOM 2231 C6 LAT 1347 24.216 53.701 68.651 1.00 23.05 ATOM 2232 O1 LAT 1347 21.713 55.161 65.005 1.00 29.10 ATOM 2233 O2 LAT 1347 21.103 52.228 64.162 1.00 26.57 ATOM 2234 O3 LAT 1347 22.437 50.258 65.682 1.00 23.28 ATOM 2235 O4 LAT 1347 24.642 52.079 66.577 1.00 24.26 ATOM 2236 O5 LAT 1347 22.951 54.232 66.677 1.00 26.25 ATOM 2237 O6 LAT 1347 24.608 52.886 69.776 1.00 26.54 ATOM 2238 C1′ LAT 1347 20.966 59.301 65.099 1.00 32.51 ATOM 2239 C2′ LAT 1347 22.189 58.806 65.964 1.00 31.92 ATOM 2240 C3′ LAT 1347 22.654 57.435 65.390 1.00 31.34 ATOM 2241 C4′ LAT 1347 21.441 56.495 65.526 1.00 31.39 ATOM 2242 C5′ LAT 1347 20.188 56.938 64.702 1.00 32.37 ATOM 2243 C6′ LAT 1347 18.954 56.016 64.828 1.00 33.23 ATOM 2244 O1′ LAT 1347 20.519 60.547 65.593 1.00 33.36 ATOM 2245 O2′ LAT 1347 23.244 59.759 65.873 1.00 29.82 ATOM 2246 O3′ LAT 1347 23.772 56.970 66.183 1.00 32.03 ATOM 2247 O5′ LAT 1347 19.866 58.294 65.174 1.00 31.84 ATOM 2248 O6′ LAT 1347 18.076 56.261 63.749 1.00 37.37 ATOM 2249 N1 UPG 341 27.322 44.456 57.775 1.00 12.21 ATOM 2250 C2 UPG 341 27.705 43.789 56.548 1.00 12.58 ATOM 2251 N3 UPG 341 26.796 44.078 55.491 1.00 13.15 ATOM 2252 C4 UPG 341 25.580 44.942 55.533 1.00 11.78 ATOM 2253 C5 UPG 341 25.244 45.587 56.772 1.00 12.67 ATOM 2254 C6 UPG 341 26.069 45.358 57.842 1.00 12.46 ATOM 2255 O2 UPG 341 28.671 43.078 56.445 1.00 11.36 ATOM 2256 O4 UPG 341 24.924 45.060 54.495 1.00 13.21 ATOM 2257 C4* UPG 341 28.139 45.820 61.018 1.00 13.58 ATOM 2258 O4* UPG 341 27.383 44.722 60.301 1.00 11.69 ATOM 2259 C3* UPG 341 28.971 46.440 59.908 1.00 10.52 ATOM 2260 O3* UPG 341 30.005 47.173 60.471 1.00 11.62 ATOM 2261 C2* UPG 341 29.272 45.220 59.097 1.00 11.03 ATOM 2262 O2* UPG 341 30.400 44.483 59.548 1.00 9.93 ATOM 2263 C1* UPG 341 28.051 44.379 59.135 1.00 12.83 ATOM 2264 C5* UPG 341 26.814 46.217 61.487 1.00 13.32 ATOM 2265 O5* UPG 341 26.265 47.573 61.238 1.00 16.42 ATOM 2266 PA UPG 341 26.748 49.072 61.108 1.00 14.28 ATOM 2267 O1A UPG 341 28.187 49.241 61.244 1.00 14.57 ATOM 2268 O2A UPG 341 26.213 49.674 59.838 1.00 16.15 ATOM 2269 O3A UPG 341 25.983 49.214 62.459 1.00 14.41 ATOM 2270 PB UPG 341 25.800 50.467 63.365 1.00 14.57 ATOM 2271 O1B UPG 341 27.120 51.044 63.507 1.00 12.20 ATOM 2272 O2B UPG 341 24.933 51.389 62.659 1.00 14.49 ATOM 2273 O3B UPG 341 24.918 50.295 64.666 1.00 17.88 ATOM 2274 C1′ UPG 341 25.388 49.351 65.853 1.00 24.44 ATOM 2275 C2′ UPG 341 26.854 49.185 66.369 1.00 27.13 ATOM 2276 C3′ UPG 341 27.779 48.150 65.490 1.00 26.87 ATOM 2277 C4′ UPG 341 27.069 46.698 65.546 1.00 27.54 ATOM 2278 C5′ UPG 341 25.562 47.005 64.928 1.00 27.76 ATOM 2279 C6′ UPG 341 24.646 45.802 64.906 1.00 29.63 ATOM 2280 F2′ UPG 341 27.412 50.500 66.415 1.00 26.09 ATOM 2281 O3′ UPG 341 29.067 48.093 66.053 1.00 26.84 ATOM 2282 O4′ UPG 341 26.972 46.296 66.918 1.00 26.57 ATOM 2283 O5′ UPG 341 24.748 48.031 65.729 1.00 26.37 ATOM 2284 O6′ UPG 341 23.367 45.385 65.355 1.00 28.54 ATOM 2285 O HOH 512 54.673 48.356 65.523 1.00 25.15 ATOM 2286 O HOH 513 57.867 51.960 56.478 1.00 18.24 ATOM 2287 O HOH 514 25.903 36.241 53.371 1.00 23.04 ATOM 2288 O HOH 515 43.782 40.049 44.203 1.00 19.20 ATOM 2289 O HOH 516 25.269 48.689 57.913 1.00 20.10 ATOM 2290 O HOH 517 33.923 31.711 71.928 1.00 18.55 ATOM 2291 O HOH 518 30.388 30.310 61.293 1.00 22.80 ATOM 2292 O HOH 519 43.430 56.956 57.195 1.00 15.05 ATOM 2293 O HOH 520 49.150 58.809 68.184 1.00 22.34 ATOM 2294 O HOH 521 46.243 43.905 76.655 1.00 17.00 ATOM 2295 O HOH 522 26.676 56.544 69.515 1.00 16.47 ATOM 2296 O HOH 523 30.000 48.381 81.295 1.00 22.90 ATOM 2297 O HOH 524 44.731 41.738 76.380 1.00 28.37 ATOM 2298 O HOH 525 43.888 30.365 73.504 1.00 30.03 ATOM 2299 O HOH 526 38.608 33.989 82.252 1.00 31.63 ATOM 2300 O HOH 527 45.486 58.476 72.471 1.00 17.02 ATOM 2301 O HOH 528 36.439 60.989 58.566 1.00 21.83 ATOM 2302 O HOH 529 22.558 57.605 60.909 1.00 22.34 ATOM 2303 O HOH 510 22.910 48.263 67.559 1.00 27.02 ATOM 2304 O HOH 342 33.837 51.323 71.040 1.00 10.52 ATOM 2305 O HOH 343 33.436 45.012 60.346 1.00 11.03 ATOM 2306 O HOH 344 41.858 32.593 61.292 1.00 14.48 ATOM 2307 O HOH 345 30.314 40.780 63.189 1.00 10.46 ATOM 2308 O HOH 346 26.633 38.049 51.120 1.00 13.67 ATOM 2309 O HOH 347 25.661 58.468 67.699 1.00 17.94 ATOM 2310 O HOH 348 26.776 40.465 85.536 1.00 21.27 ATOM 2311 O HOH 349 34.269 66.072 73.361 1.00 16.12 ATOM 2312 O HOH 350 42.055 55.697 75.118 1.00 15.08 ATOM 2313 O HOH 351 24.932 44.993 86.462 1.00 15.36 ATOM 2314 O HOH 352 32.634 57.485 71.956 1.00 7.12 ATOM 2315 O HOH 353 41.424 63.579 62.874 1.00 10.82 ATOM 2316 O HOH 354 34.311 34.079 70.575 1.00 12.06 ATOM 2317 O HOH 355 31.944 30.308 71.197 1.00 16.77 ATOM 2318 O HOH 356 31.522 46.216 65.787 1.00 15.52 ATOM 2319 O HOH 357 34.596 56.735 75.449 1.00 12.10 ATOM 2320 O HOH 358 20.938 53.671 79.071 1.00 14.85 ATOM 2321 O HOH 359 42.846 60.054 74.844 1.00 14.85 ATOM 2322 O HOH 360 33.043 62.643 72.666 1.00 13.35 ATOM 2323 O HOH 361 31.465 47.811 83.263 1.00 19.48 ATOM 2324 O HOH 362 17.810 43.979 69.451 1.00 13.43 ATOM 2325 O HOH 363 44.880 61.186 73.189 1.00 13.38 ATOM 2326 O HOH 364 52.815 48.765 69.102 1.00 13.97 ATOM 2327 O HOH 365 20.792 39.749 57.158 1.00 11.23 ATOM 2328 O HOH 366 38.954 52.211 81.847 1.00 16.78 ATOM 2329 O HOH 367 22.941 41.574 81.754 1.00 17.53 ATOM 2330 O HOH 368 39.526 27.671 66.454 1.00 19.67 ATOM 2331 O HOH 369 13.108 47.479 74.594 1.00 15.51 ATOM 2332 O HOH 370 19.447 44.093 61.807 1.00 16.50 ATOM 2333 O HOH 371 30.399 40.374 82.936 1.00 9.51 ATOM 2334 O HOH 372 19.157 32.432 71.731 1.00 21.71 ATOM 2335 O HOH 374 40.516 58.977 78.099 1.00 16.53 ATOM 2336 O HOH 375 25.173 34.444 79.349 1.00 15.37 ATOM 2337 O HOH 376 46.578 58.693 67.532 1.00 13.15 ATOM 2338 O HOH 377 14.471 52.264 70.498 1.00 18.62 ATOM 2339 O HOH 378 39.660 63.544 78.200 1.00 16.08 ATOM 2340 O HOH 379 55.295 50.486 64.035 1.00 16.60 ATOM 2341 O HOH 381 48.181 45.311 54.971 1.00 17.29 ATOM 2342 O HOH 382 43.505 31.236 76.092 1.00 19.33 ATOM 2343 O HOH 383 32.590 44.068 37.933 1.00 27.84 ATOM 2344 O HOH 384 37.969 40.917 41.166 1.00 21.67 ATOM 2345 O HOH 385 31.948 51.058 85.079 1.00 18.57 ATOM 2346 O HOH 386 28.224 60.122 88.185 1.00 23.70 ATOM 2347 O HOH 387 45.297 40.751 78.746 1.00 19.73 ATOM 2348 O HOH 389 18.713 51.902 66.002 1.00 16.80 ATOM 2349 O HOH 390 24.809 39.213 56.261 1.00 19.74 ATOM 2350 O HOH 391 38.859 65.613 79.857 1.00 21.35 ATOM 2351 O HOH 392 23.682 28.524 65.843 1.00 25.37 ATOM 2352 O HOH 393 30.619 45.293 47.694 1.00 19.83 ATOM 2353 O HOH 395 16.069 54.647 63.765 1.00 21.81 ATOM 2354 O HOH 396 26.626 51.713 89.753 1.00 22.40 ATOM 2355 O HOH 397 28.064 49.899 39.247 1.00 26.58 ATOM 2356 O HOH 398 47.650 50.646 79.240 1.00 25.75 ATOM 2357 O HOH 399 27.302 61.880 78.488 1.00 23.12 ATOM 2358 O HOH 401 52.702 53.348 61.415 1.00 15.81 ATOM 2359 O HOH 402 41.238 60.307 45.671 1.00 21.78 ATOM 2360 O HOH 403 48.221 59.205 72.644 1.00 20.33 ATOM 2361 O HOH 404 32.922 39.506 83.843 1.00 26.81 ATOM 2362 O HOH 405 33.647 51.875 54.608 1.00 26.78 ATOM 2363 O HOH 406 34.729 27.098 73.772 1.00 24.68 ATOM 2364 O HOH 407 47.014 45.510 42.850 1.00 28.16 ATOM 2365 O HOH 409 46.142 41.147 44.690 1.00 22.35 ATOM 2366 O HOH 410 12.827 43.035 64.396 1.00 17.06 ATOM 2367 O HOH 411 45.907 38.504 58.159 1.00 25.94 ATOM 2368 O HOH 414 29.975 27.632 68.843 1.00 21.59 ATOM 2369 O HOH 416 49.328 45.517 72.009 1.00 16.75 ATOM 2370 O HOH 417 37.408 65.908 57.617 1.00 27.94 ATOM 2371 O HOH 418 43.941 57.374 74.443 1.00 14.75 ATOM 2372 O HOH 419 29.018 46.583 79.445 1.00 10.62 ATOM 2373 O HOH 420 28.318 58.314 71.194 1.00 13.85 ATOM 2374 O HOH 421 17.267 52.333 63.327 1.00 23.92 ATOM 2375 O HOH 422 11.697 46.878 72.387 1.00 18.34 ATOM 2376 O HOH 423 25.498 40.253 50.998 1.00 13.87 ATOM 2377 O HOH 424 17.533 50.046 67.514 1.00 16.25 ATOM 2378 O HOH 425 14.824 50.534 68.599 1.00 21.93 ATOM 2379 O HOH 426 45.832 63.034 71.218 1.00 26.79 ATOM 2380 O HOH 429 54.376 51.863 65.883 1.00 18.45 ATOM 2381 O HOH 430 50.977 47.216 76.379 1.00 23.22 ATOM 2382 O HOH 431 42.874 53.348 76.065 1.00 19.36 ATOM 2383 O HOH 432 43.449 34.666 60.899 1.00 17.96 ATOM 2384 O HOH 433 34.130 67.571 75.561 1.00 24.13 ATOM 2385 O HOH 434 27.453 42.471 87.224 1.00 32.46 ATOM 2386 O HOH 435 52.158 48.653 66.492 1.00 20.64 ATOM 2387 O HOH 436 34.404 47.778 83.422 1.00 19.34 ATOM 2388 O HOH 437 25.914 58.255 60.777 1.00 23.62 ATOM 2389 O HOH 438 24.526 68.909 75.214 1.00 33.24 ATOM 2390 O HOH 440 28.786 26.819 61.937 1.00 25.45 ATOM 2391 O HOH 441 41.960 34.523 52.538 1.00 19.68 ATOM 2392 O HOH 442 53.720 46.358 69.854 1.00 21.67 ATOM 2393 O HOH 445 28.804 38.524 84.456 1.00 25.60 ATOM 2394 O HOH 446 43.669 62.480 59.056 1.00 24.50 ATOM 2395 O HOH 447 13.951 50.958 82.440 1.00 34.99 ATOM 2396 O HOH 448 36.623 67.353 73.056 1.00 18.09 ATOM 2397 O HOH 449 23.895 37.020 54.976 1.00 23.23 ATOM 2398 O HOH 450 31.251 53.568 87.928 1.00 24.41 ATOM 2399 O HOH 452 21.273 33.232 57.364 1.00 24.12 ATOM 2400 O HOH 453 30.982 60.462 63.192 1.00 31.37 ATOM 2401 O HOH 454 45.825 39.919 74.932 1.00 33.02 ATOM 2402 O HOH 458 47.378 51.451 51.491 1.00 28.58 ATOM 2403 O HOH 459 42.709 47.306 81.851 1.00 31.79 ATOM 2404 O HOH 461 31.207 27.302 65.372 1.00 22.14 ATOM 2405 O HOH 462 28.964 26.675 71.181 1.00 28.72 ATOM 2406 O HOH 463 39.686 64.266 81.983 1.00 31.45 ATOM 2407 O HOH 466 42.215 44.109 85.084 1.00 39.24 ATOM 2408 O HOH 469 43.225 37.756 80.665 1.00 31.08 ATOM 2409 O HOH 477 33.002 24.938 70.787 1.00 44.27 ATOM 2410 O HOH 497 47.753 62.512 67.276 1.00 31.26 ATOM 2411 O HOH 611 14.151 39.876 64.132 1.00 26.85 ATOM 2412 O HOH 612 41.690 31.049 59.011 1.00 25.32 ATOM 2413 O HOH 613 52.238 45.010 68.097 1.00 25.29 ATOM 2414 O HOH 614 41.963 62.794 78.957 1.00 25.34 ATOM 2415 O HOH 615 18.316 43.721 58.649 1.00 23.51 ATOM 2416 O HOH 616 30.695 46.612 87.680 1.00 32.98 ATOM 2417 O HOH 617 24.606 40.630 48.428 1.00 28.20 ATOM 2418 O HOH 618 41.654 52.764 78.344 1.00 27.63 ATOM 2419 O HOH 620 45.215 49.791 80.776 1.00 31.54 ATOM 2420 O HOH 621 33.859 53.902 56.156 1.00 28.15 ATOM 2421 O HOH 622 36.203 37.715 83.838 1.00 31.32 ATOM 2422 O HOH 623 20.511 54.964 81.434 1.00 30.95 ATOM 2423 O HOH 624 44.439 51.283 46.458 1.00 27.81 ATOM 2424 O HOH 625 26.468 26.377 71.132 1.00 27.97 ATOM 2425 O HOH 626 41.327 54.925 84.791 1.00 35.97 ATOM 2426 O HOH 627 50.663 46.031 56.545 1.00 33.15 ATOM 2427 O HOH 628 49.607 45.005 75.531 1.00 29.21 ATOM 2428 O HOH 530 49.701 50.415 80.874 1.00 34.92 ATOM 2429 O HOH 531 29.995 55.495 89.602 1.00 30.40 ATOM 2430 O HOH 532 18.278 55.827 85.115 1.00 29.80 ATOM 2431 O HOH 533 34.321 52.394 85.636 1.00 31.13 ATOM 2432 O HOH 534 17.335 58.634 66.816 1.00 32.18 ATOM 2433 O HOH 535 37.008 41.209 84.114 1.00 33.40 ATOM 2434 O HOH 536 22.018 35.145 55.681 1.00 33.42 ATOM 2435 O HOH 537 23.707 41.537 52.919 1.00 35.31 ATOM 2436 O HOH 538 21.046 31.384 65.966 1.00 29.47 ATOM 2437 O HOH 543 20.341 47.928 87.042 1.00 29.97 ATOM 2438 O HOH 545 37.912 28.687 70.597 1.00 29.70 ATOM 2439 O HOH 546 22.366 34.826 80.821 1.00 30.63 ATOM 2440 O HOH 547 47.995 43.524 52.725 1.00 39.01 ATOM 2441 O HOH 548 41.270 50.998 82.378 1.00 34.24 ATOM 2442 O HOH 550 14.319 46.589 53.840 1.00 33.32 ATOM 2443 O HOH 552 34.230 42.579 42.029 1.00 29.38 ATOM 2444 O HOH 554 26.628 36.503 48.890 1.00 28.95 ATOM 2445 O HOH 557 25.845 65.038 64.799 1.00 31.69 ATOM 2446 O HOH 560 13.335 52.360 50.917 1.00 34.81 ATOM 2447 O HOH 561 24.566 50.832 53.862 1.00 29.06 ATOM 2448 O HOH 562 15.990 59.624 77.366 1.00 35.62 ATOM 2449 O HOH 563 36.875 51.110 84.792 1.00 36.48 ATOM 2450 O HOH 565 33.575 33.855 50.824 1.00 33.97 ATOM 2451 O HOH 570 22.705 37.189 50.422 1.00 34.04 ATOM 2452 O HOH 582 33.723 54.774 87.078 1.00 20.22 ATOM 2453 O HOH 583 31.373 44.992 62.477 1.00 31.80 ATOM 2454 O HOH 584 23.792 53.593 49.409 1.00 35.49 END

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1 7 1 310 PRT N. meningitidis 1 Met Asp Ile Val Phe Ala Ala Asp Asp Asn Tyr Ala Ala Tyr Leu Cys 1 5 10 15 Val Ala Ala Lys Ser Val Glu Ala Ala His Pro Asp Thr Glu Ile Arg 20 25 30 Phe His Val Leu Asp Ala Gly Ile Ser Glu Ala Asn Arg Ala Ala Val 35 40 45 Ala Ala Asn Leu Arg Gly Gly Gly Asn Ile Arg Phe Ile Asp Val Asn 50 55 60 Pro Glu Asp Phe Ala Gly Phe Pro Leu Asn Ile Arg His Ile Ser Ile 65 70 75 80 Thr Thr Tyr Ala Arg Leu Lys Leu Gly Glu Tyr Ile Ala Asp Cys Asp 85 90 95 Lys Val Leu Tyr Leu Asp Ile Asp Val Leu Val Arg Asp Ser Leu Lys 100 105 110 Pro Leu Trp Asp Thr Asp Leu Gly Asp Asn Trp Leu Gly Ala Cys Ile 115 120 125 Asp Leu Phe Val Glu Arg Gln Asn Ala Tyr Lys Gln Lys Ile Gly Met 130 135 140 Ala Asp Gly Glu Tyr Tyr Phe Asn Ala Gly Val Leu Leu Ile Asn Leu 145 150 155 160 Lys Lys Trp Arg Gln His Asp Ile Phe Lys Met Ala Cys Glu Trp Val 165 170 175 Glu Gln Tyr Lys Asp Val Met Gln Tyr Gln Asp Gln Asp Ile Leu Asn 180 185 190 Gly Leu Phe Lys Gly Gly Val Cys Tyr Ala Asn Ser Arg Phe Asn Phe 195 200 205 Met Pro Thr Asn Asp Ala Phe Met Ala Asn Arg Phe Ala Ser Arg His 210 215 220 Thr Asp Pro Leu Tyr Arg Asp Arg Thr Tyr Thr Ala Met Pro Val Ala 225 230 235 240 Val Ser His Tyr Cys Gly Pro Ala Lys Pro Trp His Arg Asp Cys Thr 245 250 255 Ala Trp Gly Ala Glu Arg Phe Thr Glu Leu Ala Gly Ser Leu Thr Ser 260 265 270 Val Pro Glu Glu Trp Arg Gly Lys Leu Ala Val Pro His Arg Val Phe 275 280 285 Pro Thr Lys Arg Met Leu Gln Arg Trp Arg Arg Lys Leu Ser Ala Arg 290 295 300 Phe Leu Arg Lys Ile Tyr 305 310 2 256 PRT N. gonorrhoeae 2 Met Asp Ile Val Phe Ala Ala Asp Asp Asn Tyr Ala Ala Tyr Leu Cys 1 5 10 15 Val Ala Ala Lys Ser Val Glu Ala Ala His Pro Asp Thr Glu Ile Arg 20 25 30 Phe His Val Leu Asp Ala Gly Ile Ser Glu Glu Asn Arg Ala Ala Val 35 40 45 Ala Ala Asn Leu Arg Gly Gly Gly Asn Ile Arg Phe Ile Asp Val Asn 50 55 60 Pro Glu Asp Phe Ala Gly Ser Pro Leu Asn Ile Arg His Ile Ser Ile 65 70 75 80 Thr Thr Tyr Ala Arg Leu Lys Leu Gly Glu Tyr Ile Ala Asp Cys Asp 85 90 95 Lys Val Leu Tyr Leu Asp Thr Asp Val Leu Val Arg Asp Gly Leu Lys 100 105 110 Pro Leu Trp Asp Thr Asp Leu Gly Gly Asn Trp Val Gly Ala Cys Ile 115 120 125 Asp Leu Phe Val Glu Arg Gln Glu Gly Tyr Lys Gln Lys Ile Gly Met 130 135 140 Ala Asp Gly Gly Val Cys Tyr Ala Asn Ser Arg Phe Asn Phe Met Pro 145 150 155 160 Thr Asn Tyr Ala Phe Met Ala Asn Gly Phe Ala Ser Arg His Thr Asp 165 170 175 Pro Leu Tyr Leu Asp Arg Thr Asn Thr Ala Met Pro Val Ala Val Ser 180 185 190 His Tyr Cys Gly Ser Ala Lys Pro Trp His Arg Asp Cys Thr Val Trp 195 200 205 Gly Ala Glu Arg Phe Thr Glu Leu Ala Gly Ser Leu Thr Thr Val Pro 210 215 220 Glu Glu Trp Arg Gly Lys Leu Ala Val Pro Pro Thr Lys Cys Met Leu 225 230 235 240 Gln Arg Trp Arg Lys Lys Leu Ser Ala Arg Phe Leu Arg Lys Ile Tyr 245 250 255 3 302 PRT P. multocia 3 Met Asn Ile Leu Phe Val Ser Asp Asp Val Tyr Ala Lys His Leu Val 1 5 10 15 Val Ala Ile Lys Ser Ile Ile Asn His Asn Glu Lys Gly Ile Ser Phe 20 25 30 Tyr Ile Phe Asp Leu Gly Ile Lys Asp Glu Asn Lys Arg Asn Ile Asn 35 40 45 Asp Ile Val Ser Ser Tyr Gly Ser Glu Val Asn Phe Ile Ala Val Asn 50 55 60 Glu Lys Glu Phe Glu Ser Phe Pro Val Gln Ile Ser Tyr Ile Ser Leu 65 70 75 80 Ala Thr Tyr Ala Arg Leu Lys Ala Ala Glu Tyr Leu Pro Asp Asn Leu 85 90 95 Asn Lys Ile Ile Tyr Leu Asp Val Asp Val Leu Val Phe Asn Ser Leu 100 105 110 Glu Met Leu Trp Asn Val Asp Val Asn Asn Phe Leu Thr Ala Ala Cys 115 120 125 Tyr Asp Ser Phe Ile Glu Asn Glu Lys Ser Glu His Lys Lys Ser Ile 130 135 140 Ser Met Ser Asp Lys Glu Tyr Tyr Phe Asn Ala Gly Val Met Leu Pro 145 150 155 160 Asn Leu Asp Glu Trp Arg Lys Met Asp Val Phe Ser Arg Ala Leu Gln 165 170 175 Leu Leu Ala Met Tyr Pro Asn Gln Met Ile Tyr Gln Asp Gln Asp Ile 180 185 190 Leu Asn Ile Leu Phe Arg Asn Lys Val Cys Tyr Leu Asp Cys Arg Phe 195 200 205 Asn Phe Met Pro Asn Gln Leu Glu Arg Ile Lys Gln Tyr His Lys Gly 210 215 220 Lys Leu Ser Asn Leu His Ser Leu Glu Lys Thr Thr Met Pro Val Val 225 230 235 240 Ile Ser His Tyr Cys Gly Pro Glu Lys Ala Trp His Ala Asp Cys Lys 245 250 255 His Phe Asn Val Tyr Phe Tyr Gln Lys Ile Leu Ala Glu Ile Thr Arg 260 265 270 Gly Thr Asp Lys Glu Arg Val Leu Ser Ile Lys Thr Tyr Leu Lys Ala 275 280 285 Leu Ile Arg Arg Ile Arg Tyr Lys Phe Lys Tyr Gln Val Tyr 290 295 300 4 330 PRT H. influenzae 4 Met Thr Asp Arg Gln Thr Asp Arg Gln Thr Asp Arg Gln Thr Asp Arg 1 5 10 15 Gln Thr Asp Arg Gln Thr Asp Arg Gln Thr Asp Arg Gln Thr Asp Gly 20 25 30 Arg Thr Val Ser Gln Thr Met Asn Ile Ile Phe Ser Ser Asp His Tyr 35 40 45 Tyr Ala Pro Tyr Leu Ala Val Ser Ile Phe Ser Ile Ile Lys His Thr 50 55 60 Pro Lys Lys Ile Asn Phe Tyr Ile Leu Asp Met Lys Ile Asn Gln Glu 65 70 75 80 Asn Lys Thr Ile Ile Asn Asn Leu Ala Ser Ala Tyr Ser Cys Lys Val 85 90 95 Phe Phe Leu Pro Val Cys Glu Ser Asp Phe Gln Asn Phe Pro Lys Thr 100 105 110 Ile Asp Tyr Ile Ser Leu Ala Thr Tyr Ala Arg Leu Asn Leu Thr Lys 115 120 125 Tyr Ile Lys Asn Ile Asp Lys Ala Ile Tyr Ile Asp Val Asp Thr Leu 130 135 140 Thr Asn Ser Ser Leu Gln Glu Leu Trp Asn Ile Asp Ile Thr Asn Tyr 145 150 155 160 Tyr Leu Ala Ala Cys Arg Asp Thr Phe Ile Asp Val Lys Asn Glu Ala 165 170 175 Trp Lys Lys Thr Ile Gly Leu Glu Gly Tyr Ser Tyr Phe Asn Ala Gly 180 185 190 Ile Leu Leu Ile Asn Leu Asn Lys Trp Lys Glu Glu Asn Ile Phe Gln 195 200 205 Lys Ser Ile Asn Trp Met Asn Lys Tyr Asn Asn Val Met Lys Tyr Gln 210 215 220 Asp Gln Asp Ile Leu Asn Gly Ile Cys Lys Gly Lys Val Lys Phe Ile 225 230 235 240 Asn Asn Arg Phe Asn Phe Thr Pro Thr Asp Arg Asp Leu Ile Lys Lys 245 250 255 Lys Asn Leu Leu Cys Val Lys Met Pro Ile Val Ile Ser His Tyr Cys 260 265 270 Gly Pro Asn Lys Phe Trp His Lys Lys Cys Ser His Leu Asn Cys His 275 280 285 Ile Gly Asn Leu Leu Leu Lys Glu Met Asp Lys Ile Ile Asp Ile Pro 290 295 300 Ser Ser Trp Tyr Asp His Phe Glu Lys Ile Pro Phe Leu Ile Lys Ile 305 310 315 320 Lys Arg Leu Arg Lys Arg Ile Lys Asp His 325 330 5 338 PRT E. coli 5 Met Ser Ala His Tyr Phe Asn Pro Gln Glu Met Ile Asn Lys Thr Ile 1 5 10 15 Ile Phe Asp Glu Arg Pro Ala Ala Ser Val Ala Ser Ser Phe His Val 20 25 30 Ala Tyr Gly Ile Asp Lys Asn Phe Leu Phe Gly Cys Gly Val Ser Ile 35 40 45 Thr Ser Val Leu Leu His Asn Asn Asp Val Ser Phe Val Phe His Val 50 55 60 Phe Ile Asp Asp Ile Pro Glu Ala Asp Ile Gln Arg Leu Ala Gln Leu 65 70 75 80 Ala Lys Ser Tyr Arg Thr Cys Ile Gln Ile His Leu Val Asn Cys Glu 85 90 95 Arg Leu Lys Ala Leu Pro Thr Thr Lys Asn Trp Ser Ile Ala Met Tyr 100 105 110 Phe Arg Phe Val Ile Ala Asp Tyr Phe Ile Asp Gln Gln Asp Lys Ile 115 120 125 Leu Tyr Leu Asp Ala Asp Ile Ala Cys Gln Gly Asn Leu Lys Pro Leu 130 135 140 Ile Thr Met Asp Leu Ala Asn Asn Val Ala Ala Val Val Thr Glu Arg 145 150 155 160 Asp Ala Asn Trp Trp Ser Leu Arg Gly Gln Ser Leu Gln Cys Asn Glu 165 170 175 Leu Glu Lys Gly Tyr Phe Asn Ser Gly Val Leu Leu Ile Asn Thr Leu 180 185 190 Ala Trp Ala Gln Glu Ser Val Ser Ala Lys Ala Met Glu Met Leu Ala 195 200 205 Asp Lys Ala Ile Val Ser Arg Leu Thr Tyr Met Asp Gln Asp Ile Leu 210 215 220 Asn Leu Ile Leu Leu Gly Lys Val Lys Phe Ile Asp Ala Lys Tyr Asn 225 230 235 240 Thr Gln Phe Ser Leu Tyr Asn Glu Leu Lys Lys Ser Phe Val Cys Pro 245 250 255 Ile Asn Asp Glu Thr Val Ile Ile His Tyr Val Gly Pro Thr Lys Pro 260 265 270 Trp His Tyr Trp His Glu Tyr Pro Ser Ala Gln Pro Phe Ile Lys Ala 275 280 285 Lys Glu Ala Ser Pro Trp Lys Asn Glu Pro Leu Met Arg Pro Val Asn 290 295 300 Ser Asn Tyr Ala Arg Tyr Cys Ala Lys His Asn Phe Lys Gln Asn Lys 305 310 315 320 Pro Ile Asn Gly Ile Met Asn Tyr Ile Tyr Tyr Phe Tyr Leu Lys Ile 325 330 335 Ile Lys 6 337 PRT S. typhimurium 6 Met Ser Arg Lys Tyr Phe Glu Glu Glu Val Ile Gln Gln Thr Leu Asp 1 5 10 15 Tyr Asn Tyr Ala Gln His Ser Asp Ala Asp Lys Phe Asn Ile Ala Tyr 20 25 30 Gly Ile Asp Lys Asn Phe Leu Phe Gly Cys Gly Val Ser Ile Ala Ser 35 40 45 Val Leu Leu Ala Asn Pro Glu Lys Ala Leu Ala Phe His Val Phe Thr 50 55 60 Asp Phe Phe Asp Glu Glu Asp Gln Gln Arg Phe Glu Ala Leu Ala Lys 65 70 75 80 Gln Trp Ala Thr Gln Ile Val Val Tyr Leu Ile Asp Cys Glu Arg Leu 85 90 95 Lys Ser Leu Pro Ser Thr Lys Asn Trp Thr Tyr Ala Thr Tyr Phe Arg 100 105 110 Phe Ile Ile Ala Asp Tyr Ser Asp Lys Thr Asp Arg Glu Val Leu Tyr 115 120 125 Leu Asp Ala Asp Ile Ala Cys Lys Gly Ser Leu Gln Glu Leu Ile Asp 130 135 140 Leu Asn Phe Ala Glu Asn Glu Ile Ala Ala Val Val Ala Glu Gly Glu 145 150 155 160 Leu Glu Trp Trp Thr Lys Arg Ser Val Ser Leu Ala Thr Pro Gly Leu 165 170 175 Val Ser Gly Tyr Phe Asn Ala Gly Phe Ile Leu Ile Asn Ile Pro Leu 180 185 190 Trp Thr Ala Glu Asn Ile Ser Lys Lys Ala Ile Glu Met Leu Lys Asp 195 200 205 Pro Gln Val Val Gln Arg Ile Thr His Leu Asp Gln Asp Val Leu Asn 210 215 220 Ile Phe Leu Val Asn Lys Ala Arg Phe Val Asp Lys Lys Phe Asn Thr 225 230 235 240 Gln Phe Ser Leu Asn Tyr Glu Leu Lys Asp Ser Val Ile Asn Pro Val 245 250 255 Asp Ala Glu Thr Val Phe Val His Tyr Ile Gly Pro Thr Lys Pro Trp 260 265 270 His Ser Trp Gly Ala Tyr Pro Val Ser Gln Tyr Phe Leu Gln Ala Lys 275 280 285 Ser Asn Ser Pro Trp Ser His Cys Ala Leu Leu Asn Pro Val Thr Ser 290 295 300 His Gln Leu Arg Tyr Ala Ala Lys His Met Phe Asn Gln Lys His Trp 305 310 315 320 Thr Ser Gly Ile Asn Tyr Tyr Ile Ala Tyr Ile Lys Arg Lys Leu Leu 325 330 335 Glu 7 371 PRT H. pyroll 7 Met Ser Ile Ile Ile Pro Ile Val Ile Ala Phe Asp Asn His Tyr Ala 1 5 10 15 Met Pro Ala Gly Val Ser Leu Tyr Ser Met Leu Ala Cys Ala Lys Thr 20 25 30 Glu His Pro Gln Ser Gln Asn Asp Ser Glu Lys Leu Phe Tyr Lys Ile 35 40 45 His Cys Leu Val Asp Asn Leu Ser Leu Glu Asn Gln Ser Lys Leu Lys 50 55 60 Glu Thr Leu Ala Pro Phe Ser Ala Phe Ser Ser Leu Glu Phe Leu Asp 65 70 75 80 Ile Ser Thr Pro Asn Leu His Ala Thr Pro Ile Glu Pro Ser Ala Ile 85 90 95 Asp Lys Ile Asn Glu Ala Phe Leu Gln Leu Asn Ile Tyr Ala Lys Thr 100 105 110 Arg Phe Ser Lys Met Val Met Cys Arg Leu Phe Leu Ala Ser Leu Phe 115 120 125 Pro Asp Tyr Asp Lys Ile Ile Met Phe Asp Ala Asp Thr Leu Phe Leu 130 135 140 Asn Asp Val Ser Glu Ser Phe Phe Ile Pro Leu Asp Gly Tyr Tyr Phe 145 150 155 160 Gly Ala Lys Asp Phe Ala Ser Asp Lys Ser Pro Lys His Phe Gln Ile 165 170 175 Val Arg Glu Lys Asp Pro Arg Gln Ala Phe Ser Leu Tyr Glu His Tyr 180 185 190 Leu Asn Glu Ser Asp Met Gln Ile Ile Tyr Glu Ser Asn Tyr Asn Ala 195 200 205 Gly Phe Leu Val Val Asn Leu Lys Leu Trp Arg Ala Asp His Leu Glu 210 215 220 Glu Arg Leu Leu Asn Leu Thr His Gln Lys Gly Gln Cys Val Phe Tyr 225 230 235 240 Pro Glu Gln Asp Leu Leu Thr Leu Ala Cys Tyr Gln Lys Val Leu Ile 245 250 255 Leu Pro Tyr Ile Tyr Asn Thr His Pro Phe Met Ala Asn Gln Lys Arg 260 265 270 Phe Ile Pro Asp Lys Lys Glu Ile Val Met Leu His Phe Tyr Phe Val 275 280 285 Gly Lys Pro Trp Val Leu Pro Thr Phe Ser Tyr Ser Lys Glu Trp His 290 295 300 Glu Thr Leu Leu Lys Thr Pro Phe Tyr Ala Glu Tyr Ser Val Lys Phe 305 310 315 320 Leu Lys Gln Met Thr Glu Cys Leu Ser Leu Lys Asp Lys Gln Lys Thr 325 330 335 Phe Glu Phe Leu Ala Pro Leu Leu Asn Lys Lys Thr Leu Leu Glu Tyr 340 345 350 Val Phe Phe Arg Leu Asn Arg Ile Phe Lys Arg Ile Lys Glu Lys Phe 355 360 365 Phe Asn Ser 370 

1. A crystal comprising a ligand binding pocket of a retaining glycosyltransferase enzyme.
 2. A crystal as claimed in claim 1 wherein the ligand binding pocket is capable of associating with a donor molecule or analogue thereof, or an acceptor molecule or analogue thereof.
 3. A crystal as claimed in claim 1 wherein the ligand binding pocket is capable of associating with a diphosphate group of a donor molecule, a nucleotide of a donor molecule, a heterocyclic base of a donor molecule, a sugar of a nucleotide of a donor molecule, a selected sugar of a donor molecule that is transferred to an acceptor, or an acceptor.
 4. A crystal comprising a ligand binding pocket of a glycosyltransferase and a donor molecule or analogue thereof, from which it is possible to derive structural data for the donor molecule.
 5. A crystal comprising the ligand binding pocket of a glycosyltransferase and an acceptor molecule or analogue thereof, from which it is possible to derive structural data for the acceptor molecule.
 6. A crystal as claimed in claim 1 wherein the ligand binding pocket is defined by one or more amino acid residues of a glycosyltransferase of atomic interactions shown in Table
 3. 7. A crystal as claimed in claim 1 defined by the structural coordinates of one or more atomic contacts or atomic interactions as shown in Table
 3. 8. A crystal according to any preceding claim, wherein the glycosyltransferase enzyme is capable of catalysing a step in the biosynthesis of a lipooligosaccharide.
 9. A crystal according to any preceding claim wherein the glycosyltransferase enzyme is derivable from a pathogenic microorganism.
 10. A crystal according to claim 11, wherein the glycosyltransferase enzyme is derivable from a gram negative mucosal pathogen such as one selected from the group consisting of: Neisseria, Escherichia, Salmonella, Haemophilus, Moraxella, Bordatella, and Campylobacter.
 11. A crystal according to any preceding claim, wherein the glycosyltransferase enzyme is a galactosyltransferase.
 12. A crystal according to claim 7, wherein the galactosyltransferase is α-1,4-galactosyltransferase derivable from Neisseria meningitidis.
 13. A crystal according to any preceding claim wherein the crystal comprises a glycosyltransferase enzyme having a mutation in the part of the enzyme which is involved in attachment to bacterial membranes.
 14. A crystal according to any preceding claim wherein the crystal comprises a glycosyltransferase enzyme having a mutation in one or more cysteine residues.
 15. A crystal according to any preceding claim, wherein the ligand binding pocket is complexed with a donor molecule or analogue thereof
 16. A crystal according to claim 15, wherein the ligand binding pocket is complexed with UDP-2FGal.
 17. A crystal according to claim 15 or 16, wherein the donor molecule or analogue thereof interacts with a loop comprising residues 75-80 and a loop comprising residues 246-251 of the glycosyltansferase enzyme.
 18. A crystal according to any preceding claim wherein UDP-Gal is capable of acting as a donor molecule for the glycosyltransferase enzyme, and wherein the ligand binding pocket comprises at least one of the residues involved in binding to the UDP portion of UDP-Gal, namely: Asp 8, Ala 6, Ile 104, Lys 250, Gly 247 and His
 78. 19. A crystal according to any preceding claim wherein the ligand binding pocket comprises at least one of the residues involved in shielding the reactive center C1′ atom from water, namely: Ile 76, Asp 103, Asp 153, Ala 154, Gly 155, Tyr 186, Gln 189, His 244, Cys 246 and Gly
 247. 20. A crystal according to any preceding claim, wherein the ligand binding pocket comprises Gln
 189. 21. A crystal according to any preceding claim wherein UDP-Gal is capable of acting as a donor molecule for the glycosyltransferase enzyme, and wherein the ligand binding pocket comprises at least one of the residues involved in binding to the galactosyl moiety of UDP-Gal, namely: Asp103, Arg 86, and Asp
 188. 22. A crystal according to any preceding claim wherein the ligand binding pocket comprises at least one DXD motif.
 23. A crystal according to any preceding claim wherein the ligand binding pocket is in association with a metal cofactor.
 24. A crystal according to claim 23, wherein the metal cofactor is manganese.
 25. A crystal according to claim 24, which comprises a Mn²⁺ ion co-ordinated with the side chain atoms of His 244, Asp 103 and Asp
 105. 26. A crystal according to any preceding claim, wherein the ligand binding pocket is complexed with a acceptor molecule or analogue thereof.
 27. A crystal according to claim 26, wherein the ligand binding pocket is complexed with 4-deoxylactose.
 28. A crystal according to claim 26 or 27, wherein lactose is capable of acting as an acceptor molecule for the glycosyltransferase enzyme, and wherein the ligand binding pocket comprises at least one of the residues involved in binding to lactose, namely: Asp130, Gln 189, Val 76, His 78, Tyr 186, Cys 246, Gly 247, Phe 132, Pro 211, Pro 248, Thr 212 and Cys
 246. 29. A crystal according to any preceding claim having the structural coordinates shown in Table 4 , 5, or
 6. 30. A model of a ligand binding pocket of a glycosyltransferase enzyme made using a crystal according to any preceding claim.
 31. A crystal of a retaining glycosyltransferase comprising the structural coordinates shown in Table 4, 5, or
 6. 32. A model of a retaining glycosyltransferase made using a crystal according to claim
 31. 33. A computer-readable medium having stored thereon a crystal or model according to any preceding claim.
 34. A method of determining the secondary, tertiary, and/or quanternary structures of a polypeptide comprising the step of using a crystal or model according to any of the preceding claims.
 35. A method of screening for a ligand capable of binding to a ligand binding pocket and/or modulating the function of a retaining glycosyltransferase, comprising the use of a crystal or model according to any preceding claim.
 36. A ligand identified by a method according to claim
 35. 37. A ligand according to claim 36 which is capable of inhibiting lipooligosaccharide biosynthesis.
 38. A ligand according to claim 36 or 37 which is capable of causing oxidation of Cys
 246. 39. A method for identifying a potential modulator of a glycosyltransferase by determining binding interactions between a test compound and atomic contacts of a model of a ligand binding pocket of a glycosyltransferase as claimed in any preceding claim comprising: (a) generating the atomic contacts on a computer screen; (b) generating test compounds with their spatial structure on the computer screen; (c) determining whether the compounds associate or interact with the atomic contacts defining the glycosyltransferase; (d) identifying test compounds that are potential modulators by their ability to enter into a selected number of atomic contacts.
 40. A method for identifying a potential modulator of a glycosyltransferase function by docking a computer representation of a test compound with a computer representation of a model of a glycosyltransferase or a ligand binding pocket as claimed in any preceding claim.
 41. A method for the design of ligands for a retaining glycosyltransferase based on the crystal or model of a donor molecule or portion thereof or an acceptor or portion thereof comprising using the structural coordinates shown in Table 4, 5, or
 6. 42. A method as claimed in claim 41 comprising (a) generating a computer representation of a donor molecule or an acceptor molecule defined by the structural coordinates shown in Table 4, 5, or 6; (b) searching for molecules in a data base that are similar to the defined donor molecule or acceptor, using a searching computer program, or replacing portions of the donor molecule or acceptor molecule with similar chemical structures from a database using a compound building computer program.
 43. A modulator of a glycosyltransferase comprising a donor molecule or an acceptor molecule having the shape and structure of a donor molecule or acceptor molecule in the active site binding pocket of a reaction catalyzed by a glycosyltransferase.
 44. Use of a ligand or a modulator as claimed in any preceding claim in the manufacture of a medicament to treat and/or prevent a disease in a mammalian patient
 45. A pharmaceutical composition comprising a ligand or a modulator according to any preceding claim and optionally a pharmaceutically acceptable carrier, diluent, excipient or adjuvant or any combination thereof.
 46. A method of treating and/or preventing a disease comprising administering a ligand according to any preceding claim, and/or a pharmaceutical composition according to claim 45 to a mammalian patient.
 47. A computer for producing a model or three-dimensional representation of a molecule or molecular complex, wherein said molecule or molecular complex comprises a retaining glycosyltransferase or ligand binding pocket thereof defined by structural coordinates of a retaining glycosyltransferase amino acids or a ligand binding pocket thereof, or comprises structural coordinates of atoms of a ligand or a three-dimensional representation of a homolog of said molecule or molecular complex, wherein said computer comprises: (a) a machine-readable data storage medium comprising a data storage material encoded with machine readable data wherein said data comprises the structural coordinates of glycosyltransferase amino acids according to Table 4, 5, or 6 or a ligand binding pocket or a ligand thereof; (b) a working memory for storing instructions for processing said machine-readable data; (c) a central-processing unit coupled to said working memory and to said machine-readable data storage medium for processing said machine readable data into said three-dimensional representation; and (d) a display coupled to said central-processing unit for displaying said three-dimensional representation.
 48. A method of conducting a drug discovery business comprising: (a) providing one or more systems or methods for identifying modulators based on a model according to any preceding claim; (b) conducting therapeutic profiling of modulators identified in step (a), or further analogs thereof, for efficacy and toxicity in animals; and (c) formulating a pharmaceutical composition including one or more agents identified in step (b) as having an acceptable therapeutic profile.
 49. A method as claimed in claim 48 including establishing a distribution system for distributing the pharmaceutical composition for sale, and optionally establishing a sales group for marketing the pharmaceutical composition.
 50. A method of conducting a target discovery business comprising: (a) providing one or more system or method for identifying modulators based on a model as claimed in any preceding claim; (b) optionally conducting therapeutic profiling of modulators identified in (a) for efficacy and toxicity in animals; and (c) licensing to a third party the rights for further drug development and/or sales for agents identified in step (a), or analogs thereof.
 51. A crystal comprising a glycosyltransferase ligand binding pocket, substantially as described herein and with reference to the accompanying figures. 